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   Huntington’s
   Fragile X
   Myotonic Dystrophy
   Prader Willie
   Spinal/bulbar muscular atrophy (Fredicks ataxia)
   Aortic Arch
   Upper Esophagus
   True Vocal Cords
   Cilia
•Myositis
    •1 muscle hurts
•Polymyocytis
    •Bunch of muscles Hurt
•Dermatomyositis
    •HELIOTROPIC RASH + muscle pain
•Fibrositis
    •Muscle insertions hurt when you move them
•Fibromyalgia
    •Hurts all the time
•Polymyalgia Rheumatica
    •Weekness in the SHOULDER GURDLE…. Associated with temporal arteritis
•Temporal Arteritis
    •Macrophages eating temporal artery, ESR > 60
   RIPS

   Rifampin
   INH
   Predinsone
   -Statins
   Hypothyroidism (Hashimoto)
   Cushing disease
   T. Spiralis
   Arylsulfatase deficiency
     Metachromatic leukodystoryphy
   G6-PD
   CGD
   Pyruvate dehydrogenase Def.
   Fabry’s
   Hunter’s
   Lesch-nyhan
   Decreased Protein
     WHY?
     ▪   Decreased intake
     ▪   Cirrhosis
     ▪   Nephrotic Syndrome
     ▪   Merrentic Syndrome
   Kidneys ( at all times )
   Diabetes Mellitus
   Riley-Day Syndrome
   Shy-Dragger Syndrome
       CLUES?
        ▪ Pt. gets up and passes out
   Sick Sinus Syndrome
   Pituitary adenoma
     White nipple discharge = most likely milk due to
     increased prolactin
   Ileum
   Sigmoid Colon
   Choanal atrasia
     Turning blue on breast feeding
   C-Type Esophageal Atresia
   Duodenal Atresia
     Down syndrome
     Double bubble sign
   Pyloric stenosis
   Achalasia
   Intussuseption
     CLUES
      ▪ Knees in chest
      ▪ Sausage shaped mass
      ▪ Current jelly Stool
   Adhesions
   Internal Hernias
   Hirschsprung’s Disease
   Adhesions
   Adhesions
   Obstruction
       Cannot move stool

   Diverticulitis
   Cancer
   Mesonephrons
   Reticulonodular appearance
   May progress to Honey comb lung
   Gradual onset dyspnea, first evident only on
    exertion
   OA
   Septic Artheritis
   Crystal induced(GOUT)
   RA
   Viral
   SLE
   Ankylosing spondylitis
   Gonoccal Artheritis
   Rheumatic Fever
   Lyme Disease
   LH
   FSH
   TSH
   DM type 2
   Niacin
   HPL ( Human Placental Lactogen )
   Acanthosis Nigracan
   Because of the LIVER
   Polyhydramnios
   Reily Day Syndrome
     Baby cries but no tears
   Werdnig Hoffmann disease
     Fasciculation is a newborn
   Oligohydramnios
   CC LL S

   Chagas Disease (Whipple’s)
   C. Diptheria
   Lyme Disease
   Legionella
   Salmonella typhii (typhoid)
   CC S Y

   Crohn’s
   Chlamydia
   Shigella
   Yersina
   I AM HE

   Influenzae
   Adenovirus
   Mycoplasma
   Hepatitis C
   EBV
   H I PPPE

   Hydralazine
   INH
   Phenytoin
   Procainamide
   Penicillamine
   Ethosuximide
   ABC V

   AZT
   Benzene
   Chloramphenicol
   Vinblastine

   Vinblastine Anilate Bone Cells
   Vibrio
   Campylobacter
   Listeria
   H. pylori

   Campylobacter Has Very Long Comma Genes
   Giardia lamblia
   Corynebacterium Diptheria
     CLUES
     ▪ Grey membrane
     ▪ Inhibits EF-2
   RESPI

   Rifampin
   Ethambutanol
   Streptomycin
   Pyrazinamide
   INH
   C SSS PM
   Cryoglobinemia (I AM HE)
   Serum Sickness (Type III hypersen.)
   SLE ( ANA, Anti-ds-DNA, Anti-Smith)
   SBE ( new onset murmur )

   PSGN ( RBC cast )
   MPGN II ( NFe3)
   C (SEE) ! QT(CUTIE) BRAGS because she can induce p450

   Carbamazapine

 Quinidine
 Tetracycline

   Barbiturates
   Rifampin
   Alcohol
   Griseofulvin
   Sulfa drugs
   I Do SMACK      INH
    Quinolones      Dapsone
                    Spirolactones
                    Macrolides
                    Amiodarone
                    Cimetidine
                    Ketoconazole
                    Quinilones
   WET DumP

   Warfarin
   Estrogen
   Theophylline

   Digoxin
   u
   m
   Phenytoin
   CGD
   Chronic Granulomatous disease
   NADPH Oxidase deficiency
   Myositis
   Hepatitis
   Increased liver enzymes
   Chancroid
   Herpes
   Lymphogranuloma inguinale
   Haemophilus ducreyi
   Cystine
   Methionine
   Mercaptoethanol
   PI IG (pig)

   Prolactin
   Insulin
   Inhibin
   GH
   PI IG (pig)

   Prolactin
   Insulin
   Inhibin
   GH

   Because Cystine makes disulfide bonds
   Mercaptoethanol cuts where?
   Cuts to R of: disulfide bonds
     Cysteine
     methionine
CLAM

   Chloramphenicol
   Lactams
     Cefamandole
     Cefoperazone
   Antabuse
     disulfiram
   Metronidazole
   When do you see elevated ESR?
     Non-specific inflammation
   When do you see Falsely high ESR?
     Anemia
   When do you see Falsely LOW ESR?
     Sickle Cell Anemia
     Polycythemia
   Acute Phase Reactants?
     IL-6
   Amyloidosis
   AA
     Acute inflammatory Disease
   AB
     Alzhiemer’s Disease
   AB-2
     Chronic Renal Failure
   AE and AF
     MEN – II
   AL
     Multiple Myeloma
   Fibroblasts
     Simple scarring
   Myofibroblasts
     Wound contraction
   NEAT ASs Hooks

   Necatur americanis
   Enterobius vermicularis
   Ankylostoma duodenale
   Trichuris trichurium

   Ascaris lumbercoides
   Strongyloides
   Please      PKU
   Check       CAH(Congential Adrenal Hyperplasia)
   Before      Biotinidase
   Going       Galactosemia
   Home        Hypothyroidism
   HLA-DR2
      ▪ Narcolepsy
      ▪ Allergy
      ▪ Goodpasture’s
      ▪ MS
   HLA-DR3 ( CC D SS )
      ▪ Celiac Sprue
      ▪ Chronic Active Hepatitis
      ▪ DM,
      ▪ Sjogren’s,
      ▪ SLE,
   HLA-DR3 & 4
       IDDM(Type I)
 HLA-DR4
   Rheumatoid Arthritis,
   Pemphigus Vulgaris
 HLA-DR5
   JRA
   Pernicious Anemia
 HLA-DR7
   Nephrotic Syndrome(Steroid
    induced)
   HLA-DR 3 & B8
     Celiac Disease
   HLA-A3
     Hemochromatosis
      ▪ (ch 6, point mut.- cysteine > tyrosine)
   HLA-B8
     MG
   HLA-B13
     Psoriasis
   HLA-B27= (PAIR)
       Psoriais(only if w/arthritis)
       Postgonococcal Arthritis
       Ankylosing Spondylitis,
       IBD,
       Reiter’s,
   HLA-BW 47=
     21 alpha Hydroxylas def.(Vit.D)
   Kills helper T-cells & eosinophils
   Inhibits Macrophage migration
   Inhibits Mast cell degranulation
   Inhibits Phospholipase A
   Stimulates protein synthesis
   Stablizes endothelium
   STELS

   Salmonella (typhoid)
   TB
   EBV
   Listeria
   Syphillis
   UTI
   Spontaneous bacterial peritonitis
   Abdominal abscess
   Cholecystitis
   Ascending cholangitis
   Appendicitis
   Ceftriaxone
   Cefixime
   Cefoxine
   Ciprofloxin
   Oflaxacin
   Gatifolxacin
   Azithromycin
   Strep bovis
   Clostridium melanogosepticus
   Bacteriodes fragilis
   Clindamycin
   Metranidazole
   Cefoxitin
   Strep. Bovis
   Clostridium melanogosepticus
   K+?
   Decreases
   Na+?
   Decreases
 Cl-?
 Decreases

   pH?
   Increases
   BP?
   Increases
   Calcified CA’s
   PSAMMoma bodies

   Papillary carcinoma of the Thyroid
   Serous cyst Adenocarcinoma of the ovary
   Meningioma
   Mesothelioma
   P PUNCH

   Proteus
   Pseudomonas
   Ureaplasma urealyticum
   Nocardia species
   Cryptococcus neoformans
   H. pylori
   Struvite (90%)
   swarming
   Brain
     Microglia
   Lungs
     Type I Pneumocytes
   Liver
     Kuffler cells
   Spleen
     Reticuloendothelial Cells (RES Cells)
   Peyer’s patch
     M-Cells
   Blood
     Monocytes
   Kidney
     Mesangal Cells
   Bone
     Osteoclast
   Lymph Node
     Dendritic Cells
   Skin
     Langerhan Cells
   Connective tissue
     Epithelioid
     Giant cells
     Histiocyte
   Intractable pain
   Hemorrhage (massive)
   Obstruction (from scarring)
   Perforation
   Adriamycin (Doxyrubicin)
   Phen-fen
   Dozaroxsin
   #1 = Virus
   #2 = Drugs
   High Fever
   Rose spots (rash)
   Intestinal fire
 Some          *Strep. Pneumo (gr+) MC
 Strange       Salmonella
 Killers
                Klebsiella
 Have
 Pretty
                H. influenza
 Nice          Pseudomonas
 Capsules      Neisseria
                Cryptococcus
   Spleen
     Think!!! splenectomy pt. with infections
   SubQ nodules
   Polyarthritis
   Erythema marginatum
   Carditis
   Chorea
   Neoplasms
   Allergies/Asthma
   Addison’s Dz
   Collagen Vascular Dz
   Parasites
B.S HAVE CASH

   Benzene
   Schistomiasis

   Hep B,C,D
   Aflatoxin
   Vinyl chloride
   Ethanol

   Carbon Tetrachloride
   Anyline Dyes
   Smoking
   Hemochromatosis
   MMR OR SBYV
   Measles
   Mumps
   Rubella
   Oral Polio (sabin)
   Rotavirus
   Small pox
   BCG
   Yellow fever
   Varicella
   RIP Always    Rubella
                  Influenza
                  Polio ( salK ) [Killed]
                  HAV
   Henoch-Schoenlein P. (HSP)
   Alport’s
   Berger’s
   PCN
   α-methyldopa
   Cephalosporins
   Sulfa
   PTU
   Anti-malarials
   Dapsone
   ASA
   Heparin
   Quinidine
   T CAL

   Troponin I
   CKMB
   AST
   LDH flip
   T CAL

   Troponin I
     Appears     2 hrs
     Peaks       2 days
     Gone        7 days
   T CAL

   CK-MB
     Appears    6 hrs     6 x 1 =6
     Peaks      12 hrs    6 x 2 = 12

     Gone       24 hrs    12 x 2 = 24
   T CAL

   LDH1
     Appears    1 day
     Peaks      2 days
     Gone       3 days
   HUMORAL                        CELL MEDIATED
     Blood sample                   Tissue sample ( BIOPSY)
     B-Cells &                      T-Cells and Macrophages
      Eosinophils/neutrophils        TH-1
     TH-2                           Inhibited by IL-10
     Inhibited by INF-Gamma
                                     EVERYTHING ELSE
     ALL BACTERIA                      ▪   Virus (#1 .CMV, #2. EBV)
                                        ▪   Fungus
                                        ▪   Micobaterium
                                        ▪   Protozoa
                                        ▪   Parasite
                                        ▪   neoplasm
   Brain
     Microglia
   Lungs
     Type I Pneumocytes
   Liver
     Kuffler cells
   Spleen
     Reticuloendothelial Cells (RES Cells)
   Peyer’s patch
     M-Cells
   Blood
     Monocytes
   Kidney
     Mesangal Cells
   Bone
     Osteoclast
   Lymph Node
     Dendritic Cells
   Skin
     Langerhan Cells
   Connective tissue
     Epithelioid
     Giant cells
     Histiocyte
Cell
 mediated




Humoral
immunity
   Legionella
   Pneumocysitis carinii
   H. pylori
   Bartonella henseslae (lymph node)
   Candida (yeast)
   Sulfonamides
   Sulfonylurea
   Celebrex
   *Celecoxib
   COX 2 specific
   Vioxx (Rofecoxib)
   Pyremethamin/Sulfadiazine
   Trimethoprim/Sulfamethoxazole
   Bleomycin
   Bulsufan
   Amiodarone
   Tocainide
   Chediak-Higashi
   NADPH-oxidase deficiency
   Hyperglycemia
   Hyperuricemia
   Hypovolemia
   Hypokalemia
   OH DANG      Ototoxicity
                 Hypokalemia

                 Dehydration
                 Allergy
                 Nephritis (interstitial)
                 Gout
   MR       Decrease on inspiration (^exp)

   TR       Increase on inspiration

   VSD      Decrease on inspiration (^exp)
   Brain            Mircoglia
   Lung             Type I pneumocyte
   Liver            Kupffer cell
   Spleen           RES
   Kidney           Mesangial
   Lymph nodes      Dendritic
   Skin             Langerhans
   Bone             Osteoclasts
   CT               Histiocytes or
                     Giant cells or
                     Epithelioid cells
   RC KT SSS
   Rocky Mountain Spotted Fever
   Coxsackie A (Hand/Foot & mouth dz)
   Kawasaki
   TSS
   Syphillis
   Scarlet Fever
   Staph Scalded Skin Syndrome
   Tachypnea
   Decrease pCO2
   Decrease pO2
   Increase pH
   cAMP
   cGMP
   IP3/DAG
   Ca:Calmodulin
   Ca+
   Tyrosine kinase
   NO
   It is the 90%
   Sympathetic
   CRH (cortisol)
   Catabolic
   Parasympathetic
   Anabolic
   Neurotransmitter
   GHRH
   All hypothalamic hormones xc cortisol
   Used by what and for what?
      ▪ Smooth muscle for contraction
   Used by smooth muscle for contraction by
    distention
   Used by Gastrin only
   Used by Insulins
   Used by ALL growth factors
   Nitrates
   Viagra
   ANP
   LPS
   AR
   Defect in LFA-1 integrin proteins on phagocytes
   Absent pus formation
   Delayed separation of umbilicus
   Recurrent bacterial infections
   WAS
   SCID
   CVID
   HIV
   HTLV-1
   X-linked defect in the ability to mount an IgM response to capsular
    polysaccharides
   (Aldrich = ↑ IgA)
   normal IgE levels
   low IgM levels.
   Triad of symptoms includes: (WIPE)
     recurrent pyogenic Infections,
     thrombocytopenic Purpura,
     Eczema
   IL-4
   Framshift/Nonsense mutation
   Adenosine deaminase deficiency
   T-cell>B-cell
   Bacterial infections
   Fungal infections
   Late onset
   Frameshift/Missense mutation
   Normal numbers of circulating B cells
   Tyrosine Kinase deficiency
   T-cell>B-cell
   CD4 rich
   Brain
   Testicles
   Cervix
   Blood vessels
   Amytal
   Rotenone
   Malonate
   Antimycin D
   CN-
   CO
   Chloramphenicol
   Oligomycin
   DNP
   Free Fatty acids
   Aspirin
   Physical uncoupler
   Plasma
   Urea cycle
   Collecting ducts
   Glutaminase
 Azithromycin
  1 gram po
 Ceftriazone
  250 mg im
   Azithromycin
    1 gram po
   Ketoconazole
    150mg
   Difluccan
    1 pill
   Metronidazole
    2 grams
   Metronidazole
    2 grams
 Ceftriaxone
  250 mg im
 Cefixime
  400 mg po
 Cefoxitin
  400 mg po
 Ciprofloxacin
  500 mg po
 Ofloxacin
  400 mg po
 Gatifloxacin
  400 mg im
   Phosphorylase (Pi)
   Debranching enzyme
   Alpha-1,6 –Glucosidase
   Phosphatase
   Glycogen synthase
   Branching enzyme
   Glycogen alpha-1,4 glycosyl transferase
   Glycogen alpha-1,6 glycosyl transferase
   Phosphorylase (Pi)
   pO2?
     Normal
   pCO2?
     Normal or increased
   pH?
     Decreased
   pO2?
     Decreased
   pCO2?
     Decreased
   pH?
     Increased
   Respiratory acidosis
 Fabry’s                       α – galactosidase
 Krabbe’s                      Galactosylceramide
 Gaucher’s                     β – glucocerebrosidase
 Niemann – Pick                Sphingomyelinase
 Tay-Sachs                     Hexosaminidase
 Metachromatic leukodystrophy  Arylsulfatase
 Hurler’s                      α – L – iduronidase
 Hunter’s                      Iduronidase sulfatase
   PAIR

   Psoriasis
   Ankylosing spondylitis
   IBD (Ulcerative colitis)
   Reiter’s Syndrome
   HLA-13
   Von Gierke’s      Glucose – 6 – phosphate

   Pompe’s
                      α – 1 – 4 glucosidase

   Cori’s            Debranching enzyme

   McArdle’s
                      Glycogen phosphorylase
   Pyruvate?
     Glycine
     Alanine
     Serine

   Acetyl CoA ?
     Phenylalanine
     Isoleucine
     Threonine
     Tryptophan
     Lysine
     Leucine
   Alpha-KG ?
   Glutamate
   Glutamine

   Succinyl CoA?
   Phenylalanine
   Tryptophan
   Tyrosine
   Fumerate ?
   Proline

   Oxaloacetate?
   Aspartate
   Asparigine
   Oxidation – 7 NADH – 21 ATP
   Hydration
   Oxidation - 7FADH – 14 ATP
   Thiolysis – 8 AcCoA – 96ATP
                        131 ATP – 2 (to bring it
                            in)
   pO2?
    Decreased
   pCO2?
    Decreased
   PCWP?
    Decreased (b/c it’s a pressure problem)
   Respiratory Rate?
    Increased
   pH?
    Increased
   SZ?
    Increased
   ACTH
   ADH
   PTH
   TSH
   ANP
   Anti-smith
   Anti cardiolipin
   Anti-ds DNA

     SLE
   Anti – histone?

   Drug induced SLE
   Anti-topoisomerase?

   PSS (Progressive Systemic Sclerosis)
   Anti TSH receptors?

   Graves
   Anti-centromere?

   CREST
   Anti-GBM?

   Goodpasture’s
   Type IV collagen
   Anti-mitochondria?

   Primary biliary cirrhosis
   Anti-hair follicle?

   Alopecia areata
   Anti-IgG?

   Rheumatoid arthritis
   Anti-myelin receptors?

   MS
   Anti-gliaden?
   Anti-gluten?

   Celiac sprue
   Anti-islet cell receptor?

   DM Type I
   Anti-melanocyte?

   Viteligo
   Anti-ACh receptor?

   MG
   Anti-ribonuclear protein?

   Mixed Connective Tissue dz (MCTD)
   Anti-parietal cell receptor?

   Pernicious anemia
   Intrinsic factor
   Anti-epidermal anchoring protein receptors?

   Pemphigus vulgaris
   Intercelluar junctions of epidermal cells
   Anti-epidermal basement membrane protein?

   Bullous pemphigoid
 IgG sub-epidermal blisters
 Oral blisters
   Anti-platelet?

   ITP
   Glycoprotein IIb/IIIa
   Anti-thyroglobulin?
   Anti-microsomal?

   Hashimoto’s
   Anti-smooth muscle?
   Anti-scl-70?

   Scleroderma
   Anti-rho (SS-A)?
   Anti-la?

   Sjogren’s
   Anti-proteinase?
   C-ANCA?

   Wegener’s
   P-ANCA?

   Polyarteritis nodosa
 Hepatitis   B antigen
 IgM
 Papilloma virus?
          Cervical CA
 EBV?
          Burkitts
          Nasopharyngeal CA
 HepB & C?
          Liver CA
 HIV?
          Kaposi’s Sarcoma
   Clot in front of renal artery?
     Renal artery stenosis
   Clot off whole renal artery?
     Renal failure
   Inflamed glomeruli?
     Glumerulo nephritis
   Clot in papilla?
     Papillary necrosis
   Clot off medulla?
     Interstitial nephritis
   Clot off pieces of nephron?
     Focal segmental GN (HIV, drug use association)
   Clot off lots of nephrons?
     Rapidly Progressive GN
   Min. change disease

   2 wks post URI
   Goodpasture’s
   Wilm’s tumor
   Adenocarcinoma
   Cyst
   Focal Segmental GN
   Membranous GN
   What does tPA, Streptokinase, Urokinase inhibit?
     Aminocaproic acid

   What doe Warfarin inhibit?
     Vitamin K

   What does Heparin inhibit?
     Protamine Sulfate
   IV push?
   20mg

   Drip?
   40mg
   IV push?
   750K

   Drip?
   750K
   Used ONLY for such things as:
      ▪ Feeding tubes
      ▪ Central lines
      ▪ Fistulas
   Loss of a patch of hair
   Loss of ALL hair on head “bald”
   Loss of hair on entire body “hairless”
   Pneumonitis with endocarditis = pulmonary
    infiltrate with severe eosinophilia
   PIE syndrome
 Necator americanus
 Ankylostoma duodenale
 Shistosomiasis
 Strongyloides
 Ascaris lumbricoides
 Immunocompromised
   Homocystine methyl transferase
   Methyl malonyl-coA mutase
   No male transmission
   All females pass it on
 Burn patients
 Cystic fibrosis
 DM
 Neutropenic patients
   cover 1x for Staph aureus during 1st week
   cover 2x for Pseudo after 2nd week
   Increased pO2
   Delayed opening/closing of the pulmonary value
   Increased volume in the right ventricle
   Blood transfusion
   Increased Tidal Volume
   Giving O2
   Right sided heart failure
   Pregnancy due to increase volume
   IV fluids
   ASD/VSD
   Deep breathing
   Hypernateremia
   SIADH
   Pulmonary regurge
   Pulmonary stenosis
   Right bundle branch block
   PIMP TRAP
   Pericardium
   Intracranial
   Mediastinum
   Pleural cavity
   Thighs
   Retroperitoneum
   Abdominal cavity
   Pelvis
   Gram +
   Basement membrane suppressor
   Works on simple anaerobes
   The #1 cause of anaphylaxis
   Causes interstial nepritits
   Causes nonspecific rashes
   Acts as a hapten causing hemolytic anemia
   Penicillin
   GIFTS

   Granuloma
   Ileum
   Fistula
   Transmural
   Skip Lesion
 Prodromal period before symptoms = 1-3
  weeks
 Why is there a prodromal period?
 Because must switch to positive stranded before
  replication
   Symptoms within 1 week or less
   EXCEPTIONS:
       Hanta
       Ebola
       Yellow fever
       They are -ve stranded = don’t have to switch to
        positive before replicating
   Transposition of the great arteries
   Tetrology of Fallot
   Truncus Arteriosus
   Tricuspid Atresia
   Total anomalous pulmunary Venous Return
   Hypoplastic Left heart syndrome
   Ebstein’s anomaly
   Aortic atresia
   Pulmonary atresia
   Tetrology of Fallot
   Ebstein’s Anomaly
   Hypokalemia
   Hypermagnesemia
   Hypercalcemia (except atrium)
   Hypernatremia
   Hyperkalemia
   Hypomagnasemia
   Hypocalcemia (except atrium)
   Hyponatremia
   TLCFN (Tender Loving Care For Nancy)

   TPP –         Thiamin –             B1
   Lipoic Acid –                      B4
   CoA –         Pantothenic acid –   B5
   FAD –         Riboflavin –         B2
   NAD –          Niacin –            B3
   Bruton’s Agammaglobulinemia
   CGD (NADPH def)
   DMD
   G6PD
   Hemophilia
   Lesch-Nyhan
   Vit D resist. Rickets (X-linked dominant)
   Fabrys
   Hunters
   Bruton’s agammaglobulinemia
   CVID (Common Variant Imm. Def)
   Leukemias
   Lymphomas
   SCID
   WAS
   Job Buckley Syndrome
   Bruton’s agammaglobulinemia
   SCID
   WAS
   Job Buckley Syndrome
   Scabies
   Lichen Planus
   Urticaria
   Dermatitis Herpetiformis
   L-myc?
     Small cell lung Ca

   C-myc?
     Promyelocytic leukemia (Burkitt’s lymphoma)

   N-myc?
     Neuroblastoma
     Small cell lung CA

   C-able?
     CML
     ALL
   C-myb?
     Colon CA
     AML

   C-sis ?
     Osteosarcoma
     Glioma
     Fibrosarcoma
   C-erb B2?
     Epidermal growth factor receptors

   CSF-1 ?
     Breast
   Erb-B2?
     Breast CA
     Ovarian CA
     Gastric CA

   Ret?
     Medullary CA of thyroid
     Men II & III
     Papillary carcinoma
   Ki-ras?
     Lung CA
     Colon CA

   Bcl-2?
     Burkitts
     Follicular lymphoma

   Erb?
     Retinoblastoma
   Relax hCG Is HOPE
   Relaxin
   hCG
   Inhibin
   Human placental lactogen (HPL)
   Oxytocin (drug lactation, pit gland prod it also)
   Progesterone
   Estrogen
   Severity of microscopic change
   Degree of differentiation
   Degree of dissemination of tumor
   What the surgeon sees
   Urticaria/Hives?
     Any CA, especially lymphoma
     Pagets Ds (ulcers around nipples)

   Seborrheic keratosis (waxy warts)?
     Colon CA
     HIV if sudden increase in number
     Normal with aging
   Actinic keratosis?
     Dry scaly plaques on sun-exposed skin
     Squamous Cell CA of skin

   Dermatomyositis?
     violacious, heliotropic rash, malar area
     Colon CA
   Akanthosis nigricans?
     dark lines in skin folds
     Any visceral CA
     End organ damage

   Erythema nodosum?
       ant aspect of legs, tender nodules
       Anything granulomatous
       NOT assoc. w/ bacteria
   Apo E
   Apo A
   Apo CII

   L-CAT
     lecithin cholesterol acetyl transferase
   Cholesterol
     from periphery to liver
   Apo B-100
   Apo E
   Apo C II

   Triglcyerides (95%)
   Cholesterol (5%)
   Apo B-100
   Apo E
   Apo CII

   Triglycerides (< VLDL)
   Cholesterol (>VLDL)
   Apo B-100

   Cholesterol
     from liver to tissue


   NOT a good thing!!!!!
   Apo   A
   Apo   B-48
   Apo   E
   Apo   C II
   Triglycerides from:
   GI to liver (25% of the time)
   GI to endothelium (75% of the time)
 LDL
   Clue = HEAL
   Heart?
   Machinery murmur
   Elbow?
   Fistula from dialysis in renal disease

   Abdomen/Brain?
   Von Hippel-Lindau = clot off with coils
   Increase incidence of Renal cell CA on chrom 3

   Lungs?
   Osler Weber Rendu Syndrome
   Glucose > 200
   Age > 55
   LDH >350
   AST > 250
   WBC > 16,000
   Calcium <8 mg/dl
   HCT drop > 10%
   O2 < 60 (PaO2)
   Base deficit > 4
   BUN > 5 mg/dl
   Sequestration > 6L
   CF
   Glaucoma
     Painful, red, teary eye
   Problem with sense of taste
   Metronidazole
   Clarithromycin
   Zinc deficiency
   Flushing
   Wheezing
   diarrhea
   Serotonin
     5-HIAA
   Pancreas
   Ileum
   Mnemonic: BEDS

   Botulinum
   Erythrogenic toxin
     from strep pyogenes
   Diptheria
   Salmonella/shiga like toxin
     Has O antigen
   I sprayed ORTHO on my BUNYA at the
    ARENA down in REO to kill SEGMENTED
    WORMS
   ICAMs
   Integrins
   Selectins
   Bind proteins
   Stop the leukocytes
   Bind carbohydrates
   Mediate the rolling to slow leukocytes down
   Homing of lymphocytes
     tells lymphocytes where to go
   Inflammation
   Cell-cell interaction
   Contact
   Neutrophils

   The next cells to show up are?
   B-cells

   What do B-cells make?
   IgM
M
           Σ
               Three

   IgM peaks at what day?
   14

   When does IgM leave?
   In 2 months
   IgG

   When does IgG peak?
   In 2 months

   When does IgG leave?
   In 1 year
   MEMORY
   IgG with 5x concentration
   Has the highest affinity

   When does IgG peak?
   In 5 years

   When does IgG leave?
   In 10 years
   IgG
   IgG
   IgG
   IgE

     Uh huh! You thought all of them were IgG…
   Smoking
   Alcohol
   Nitrites
   Japanese
   Smoking
   Aniline dyes
   Benzene
   Aflatoxin
   Cyclophosphamide
   Schistosomiasis
   2 diseases:
     Von Hippel-Lindau
     Tubular sclerosis
   Nitro Blue Tetrazolium test
   What is it used for?
     Screening CGD


   What does a –ve test indicate?
     +ve for the disease
   Howell-Jolly?
     Sickle cell

   Heinz?
     G-6-P-D

   Zebra?
     Niemann pick
   Donovan?
     Leishmaniasis

   Mallory?
     Alcoholism

   Negri?
     Rabies
   Councilman?
     Yellow fever


   Call-exner?
     Ovarian tumors
      ▪ granulosa origin
   Lewy?
     Parkinsons

   Pick?
     Pick’s disease


   Barr body?
     Normal female
   Aschoff?
     Rheumatic fever


   Cowdry type A inclusions?
     Herpes virus


   Auer rods?
     AML
   Globoid?
     Krabbe’s lysosomal storage disease


   Russell?
     Multiple myeloma
   Schiller-Duvall?
     Yolk sac tumor


   Basal bodies?
     Only found in smooth mm
   Mnemonic?      ACID
   Type I
     Anaphylaxis/Atopic

   Type II
     Cytotoxic (Humoral)

   Type III
     Immune complex mediation

   Type IV
     Delayed hypersensitivity/Cell mediated
   Atopic
   IgE (Asthma) binds to mast cell
   IgA activates IP3 cascade degrading mast cells
   Humoral
   What are examples of type II?
   Rh disease
   Goodpastures
   Autoimmune hemolytic Anemia
   All Autoimmune diseases
     except RA and SLE
   Ag-Ab complement
   What are examples of Type III?
   RA
   SLE
   Vasculitides
   Some GN?
   Cell mediated
   What are examples of Type IV?
   TB skin test
   Contact dermatitis
   Transplant rejection
   Appendix
   Epithalamus
   Palmaris longus
     muscle
   Pancreatic polypeptide
     hormones in F-cells
   Goodpastures
   Wegeners
   DM
   HTN
   Vasculitis
   AIDS
   Tx?
     N-acetylcysteine

   Test used to detect CF?
     Pilocarpine sweat test

   What ion does this test measure?
     Cl-

   Definitive presence of disease has a test value of what?
     >60
   What is the value in a normal person?
     <20

   What is the value in a heterozygous person?
     30 – 60

   What chromosome is the CF gene on?
     Chrom 7
   What Second messenger is used?
     IP3/DAG
   Bacillus anthracis
   Clostridium perfringens
   Clostridium tetani
   Clostridium melangosepticus

   What is the chemical in spores?
     Calcium dipocholinate
   Lactic acid
   Alpha-receptors
   Cold agglutinin testing
     IgM
   AA amyloid?
     Chronic active disease


   AL amyloid from Ig light chain?
     Myeloma
   Beta 2 microglobulin?
     Chronic hemodialysis


   AA amyloid from SAA?
     Nephrotic hereditary forms
      ▪ eg. Mediterranean fever
   Pre-albumin/transthyretin?
     Cardiomyopathic hereditary forms
      ▪ senile systemic amyloidosis
   Neuropathic hereditary syndromes
   ANP fibrils are caused by?
     Senile cardiac amyloisosis

   Cerebral amyloid in Alzheimer’s disease/Down’s?
     Cerebral amyloidosis
   Calcitonin precursors?
     Medullary CA of thyroid

   AL from light chains?
     Isolated, massive, nodular deposits
      ▪ lung, skin, urogenital tract
   Frontotemporal dementia
   Atrophy of frontal and temporal cortex with
    sparing of remaining neocortical regions
   Altered neurofilaments
   Tau protein
   ubiquitin
   Prevents pre-synaptic release of Ach

   How do babies get it?
   From spores in honey or molasses

   How do adults get it?
   From canned food
   Lethal factor – (black necrosis)
   Protective factor
   Edema factor
   Anthracis
   Cereus
   B1-selective?
     A–M
   Non-selective?
     N–Z
   Exceptions?
     Carbetalol and Labetolol are non-selective
   Problem in proximal tubule
   Can’t reabsorb
   Low energy state causing anemia
   Can be due to old tetracycline
   In the collecting duct of the kidney

   What does glutmainase help the kidney absorb?
     Ammonia if the liver fails
   Hilum
   Pelvic brim
   Entering the bladder
   SLE
   Endometrial CA
   Cervical CA
   Carbamoyl synthase I

   Where is it found 90% of the time?
     Liver


   Where is it found 10% of the time?
     Collecting duct of the kidney
-ve   charge
+ve           charge
   What is it used for?
     Reversing the effects of heparin
   T-cells and macrophages
   Schistocytes
   Decreased platelets
   Decreased RBCs
   Bleeding from mucosal surfaces
   Bleeding from skin and GI
   Petechiae
   Ecchymoses
   The following deveop:
     Clots
     DIC
     Pulmonary embolism
     DVT
     MI
     Stroke
   Tachypnea and SOB

   Most common cause of death?
     Heart failure
   Inhibits the translocation step of ribosomal
    protein synthesis
   Inhibits ribosomal peptidyl transferase in
    prokaryotes
   Inhibits elongation by binding to “A” site and
    prematurely terminating chain growth in pro
    and eukaryotes
   Causes misreading of code during initiation in
    prokaryotes
   Prevents binding of aminoacyl-t-RNA to
    ribosome on prokaryotes therefore inhibiting
    initiation
   Inhibits ribosomal peptidyl transferase in
    eukaryotes
     cell wall inhibitor
   Blocks B-subunit of RNA polymerase
   Prophylaxis for contacts of N. meningitidis
   Cell wall inhibitor
   Binds irreversibly to Phopholipase carrier
   Bacteriacidal
   Covers all gram +ves
   Linezolid
   Blocks vitamin k dependent gamma-
    carboxylation of prothrombin and factors
    2, 7, 9, 10, proteins C & S
   Blocks translation by binding the 50S subunit
   What type of hemolysis is alpha hemolysis?
   Partial hemolysis
   What color is it’s zone?
   Green
   What type of hemolysis is beta-hemolysis?
   Complete hemolysis
   What color is it’s zone
   Clear
     eg. Streptokinase

   What type of hemolysis is gamma-hemolysis?
   No hemolysis
   What color is it’s zone?
   Red
   High urine PH (??????not sure about this)
   Acidosis
   UTI s
   Stones
   Babies die < 1 yr old
   Acidosis
     urine PH = 2, normal is 5-6
   Hypokalmia
   Patients have NO carbonic anhydrase
   It is a combination of RTA I & III
   Normal urine pH
   Hypokalemia
   Seen in diabetics
   Hyperkalemia
   NO aldosterone b/c JG apparatus has infarcted
   Viridans
   Mutans
   Sanguis
   Salivarius
   Bovis
   Viridans
   Viridans
   Mutans
   HTN
   Hematuria
   RBC casts
   Increase Edema
   Increase Lipidemia
   Increase Cholesterolemia
   Increase Coagulability
   Decrease serum Albumin
   Increase urinary Albumin
   Strep. Pneumo

   What is the #2 cause?
   Hemophilus influenza

   What is the #3 cause?
   Neisseria meningitides
   Viruses

   Which are secondary to what?
   Bacterial infections

   What is the #2 method to paralyze cilia?
   Smoking
   Staph aureus
   Clostridium perfringens
   Bacillus cereus….from what?
   Fried rice
   Preformed
   Release of glycine from spinal cord

   What physical finding would you see?
   Lock jaw

   What is the tx?
   Antitoxin and Toxoid

   Where is it injected?
   Injected in different areas of body
   E. coli

   Followed by?
   Proteus

   Followed by?
   Klebsiella
   Staph saprophyticus
   Why?
   They stick things in themselves
   18-24 yoa?
   Staph saprophyticus
   Why?
   Because they stick things inside themselves
   Why no UTI’s after 24?
   Because women are use to penises and Staph saprophyticus lives
    on penis (becomes part of normal flora).
   Osteomyelitis

   Because of what?
   Collagenase
   Staph. aureus
   Shock
   Rash
   Hypotension
   E. coli
   Then?
   Proteus
   Then?
   Klebsiella
   Group B Strep (agalactiae)
   E. coli
   Listeria
   Group B Strep (Strep. Agalactiae)
   E. coli
   Listeria
   Clostridium melanogosepticus
   Strep bovis

   What color pigment is produced?
   Black
   IgG

   What about Avidity?
   IgM
   Virus inject it’s DNA into bacteria
   Virus injects it’s DNA into it bacteria in a hospital
    or nursing home setting, then becomes deadly.
   Bacteria with Pili
   Citrobacter
   Hemophilus influenza
   Neisseria
   C3
   Gram negative bacteria
   BUN
   >20

   Fractional Na+ excertion
   <1%

   Creatine
   >40
   BUN
   10-15

   Fractional Na+ excretion
   >2%

   Creatinine
   <20
   Pavementing
   Margination
   Diapediesis
   Migration
   PFK-1
   fructose-1,6-bisphosphatase

     NOT   Pyruvate Carboxlyase
   Viral

   If resistant to tx, what next?
   Fungal
   Mycobacterium
   Protozoa
   Parasite
   Neoplasm
   Step. Group B
     Strep agalactiae
   Strep. Pneumonia
   Herpes simplex virus
   Neisseria gonorrhea
   Chlyamydia
   Perivascular angiofibromata
   Primary Adrenocoritcal Insufficiency
   Ochronosis
   Allergic Granulomatosis
   Angiitis
   Ameloblastoma

   What is Ameloblast?
   Tooth material
   Regional enteritis
   Granulomatous ileitis
   Ileocolitis
   Subacute Granulomatous Thyroiditis
   Comedo Ca
   Mucolipidosis II
   MLNS
   Mucocutaneous Lymph Node Syndrome
   Interstitial cells
   Sustentacular cells
   Giant cell arteritis (granulomatous)
   Hyperviscosity syndrome
   Oral
   Trigeminal ganglia
   Genital
   Sacral plexus
   Varicella zoster
   EBV
   Mononucleosis
   Burkitt’s
   CMV
   Inclusion bodies
   Roseola
   Duke Disease
   Exanthem subitum
   Pityriasis rosea
   Kaposi’s sarcoma
   What is the MOA?
   Interferes with normal synthesis and gama
    carboxylation of Vit. K dependent clotting
    factors via vitamin K antagonism.

   Is it long or short acting?
   Long half-life
   8-10 hours to act
   Clinical use?
   Chronic anticoagulation

   Contra-indication?
   Pregnancy because it can cross the placenta
   What pathway does it affect?
   Extrinsic pathway

   What does it do to PT?
   Prolongs

   PT
   What are the toxicities?
   Bleeding
   Teratogenic
   Drug-drug interactions

   How is it activatied?
   Tissue activated
   Administration?
   po
   II
   VII
   IX
   X
   Protein C
   Protein S
   What is the MOA?
   Catalyzes the activation of antithrombin III
   Decreases thrombin and Xa

   Is it long or short acting?
   Short half-life
   Acts immediately
   Clinical use?
   Immediate anticoagulation of pulmonary
    embolism, stroke, angina, MI, DVT.

   Contra-indication?
   Can be used during pregnancy because it does
    not cross the placenta
   What pathway does it affect?
   Intrinsic pathway

   What value should you follow?
   PTT
   What are the toxicities?
   Bleeding
   Thrombocytopenia
   Drug-drug interactions

   How is it activatied?
   Blood activated
   Administration?
   I.V.

   Drug of choice for what?
   DVT
   What is good about the newer low-molecular-
    weight heparins?
   They act more on Xa
   Have better bioavailability
   Have 2 to 4 times longer half life
   Can be administered subcutaneously and
    without laboratory monitoring.
   Protamine sulfate
   Dimercaprol
   Flumazenil
   Pralidoxime
   Deferoxamine
   Naloxene
   Bicarbonate
   Doxapram
   Activates the respiratory center in the brain
   Provostatin
   Atrovastatin
   Lovastatin
   Simvastatin
   Provastatin
   Atrovastatin
   Lovastatin
   Simvastatin
   HMG-CoA reductase

   When is it most active?
   8:00pm on
   Cholestipol
   Cholestyramine

   If nothing works what do you give?
   Probucol
   Niacin
   Flushing
   Itching
   Cholestipol
   Cholestyramine
1.Pancreatitis
 Due to What?
 ETOH

2.Kidney stones
 Due to What?
 Alcohol
3.AAA
 How is this described?
 Ripping pain down back

4.Ischemic bowel
 What is symptom?
 Bloody diarrhea
   Small cell Ca of lung
   Increased intracranial pressure
   Pain (most common)
   Drugs
   Hypoxic Lung Disease/Restrictive Lung disease
   Carbamazepine
 Melanocytes
 Odontoblasts (predentin)
 Tracheal Cartilage
 EnteroCHROMOFIN Cells
 Laryngeal/Tracheal cartilage
 Parafollicular cells of thyroid - Pseudounipolar
  cells
 All Ganglion cells (Schwann, Adrenal medulla)
 Schwann Cell
 Spiral membrane of heart
   220 - age
   RTA
   Diarrhea
   Diabetic ketoacidosis (DKA)
   Parainfluenza
   Adenovirus
   Influenza
   RSV
   Bronchiolitis
   Diarrhea
   Dermatitis
   Dementia
   Death
   Cysteine
   Ornithine
   Lysine
   Arginine
   Phase 0?
   Depolarization
   Phase 1?
   No name
   Phase 2?
   Plateau phase (A-V node)
   Phase 3?
   Repolarization
   Phase 4?
   Automaticity (S-A node)
   Wider QRS
   Wider P-wave
   Longer PR interval
   Calcium oxalate (phosphate) stones
   Struvite stones
   Uric acid stones
   Cysteine stones
   Oxalate stones
   80%
   3 y/o white male?
   CF
   5 y/o black male?
   Celiac Sprue
   Adult male?
   Whipple’s
   Adult male or female?
   Crohn’s
   In 0-20 y/o?
   Malabsorptin

   What age do they die?
   Young
   What type of crystals are present?
   Calcium pyrophosphate
   Where are they found?
   Joint spaces
   Who gets it?
   Older patients M=F
   Tx?
   Colchicine
   VSD
   ASD
   PDA
   Coarctation
   VSD
   Mitral
   ASD
   PDA
   Coarctation
   Coarctation
   Pyruvate carboxylase
   PEP carboxykinase
   F-1,6 dPhosphatase
   G-6-Phosphatase
   Hexokinase
   PFK-1
   Pyruvate kinase
   Prolactin
   GH
   Nocardia
   Cryptosporidium
   Mycotic aneurysm
   Roth spots
   Janeway lesions
   Osler’s nodes
   Splinter hemorrhages
   Endocarditis
   Janeway lesions?
   Toes

   Osler’s nodes?
   Fingers

   Roth spots?
   Retina
   Strep. viridans
   Acetaminophen
   Reye Syndrome
   Pregnancy
   Alcohol
   Staph. Aureus
   Pseudomonas
   Pseudomonas
   Diptheria
   It ADP ribosylates EF2 inhibiting protein
    synthesis

   Is it Gram +/-?
   +

   Where and how does it get its exotoxin?
   From virus via transduction
   What does it cause?
   Heart block

   What do you give for Tx?
   Antitoxin
   Never scrape membrane
   Bullous?
   Staph aureus
   Pseudomonas

   Centroacinar?
   Smoking
   Distalacinar?
   Aging

   Panacinar?
   Alpha-1 antitrypsin def
   4 mo gestation?
   Yolk sac
   6 mo gestation?
   Spleen, liver, flat bones
   8 mo gestation?
   Long bones
   1 yr old?
   Long bones
   Spleen can resume erythropoieses causing
    splenomegaly
   P-wave?
   Ca+
   QRS complex?
   Na+
   S-T?
   Ca+
   T-wave?
   K+
 U-wave?
 Na+
   QRS
   Widens P-wave
   PR interval longer
D         W

                                +          A          B        A+B

                                _          C          D       C+D

                                        A+C        B+D         ALL

Sensitivity   A/A+C                 Sensitivity: Truly Diseased People      Always in the
Specificity   D/B+D                 Specificity: Truly Well People           numerator
PPV           A/A+B                 + Predictive Value: Test +ve With DZ
NPV           D/C+D
OR            AD/BC                 - Predictive Value: Tested –ve w/o DZ     A&D
                                    OR: Odds Ratio
RR            (A/All)/(C/All)       RR: Relative Risk
AR            (A/All)-(C/All)       AR: Attributed Risk
   Atrium contraction
   Phase zero
   Calcium
   AV Node
   Phase 2
   Sodium
   Septum
   Phase 2
   Sodium
   Anterior wall
   Phase 2
   Sodium
   Posterior wall
   Phase 2
   Sodium
   Ventricle
   Phase 2
   Calcium
   Ventricle
   Phase 3
   Potassium
   Ventricle
   Phase 4
   Sodium
   Narcolepsy
   Allergy (hay fever)
   Goodpasture
   MS
   DM
   Chronic active Hepititis
   Sjogrens
   SLE
   Celiac sprue
   IDDM (DM Type 1)
   Rheumatoid Arthritis
   Pemphigus Vulgaris
   JRA (JUV RA)
   Pernicious anemia
   Nephrotic syndrome (Steroid induced)
   Celiac Disease
   Hemochromatosis
     chromosome 6
     point mutation Cystine to Tyrosine
   Myasthenia gravis
   Psoriasis
   Psoriasis
     only if with arthritis
   Ankylosing Spondylities
   IBD
     Ulcerative Cholitis
   Reiter’s
   Post gonococcal arthritis
   21 alpha hydroxylase deficiency
     Vit. D
   ADP ribosylates EF-2
   Stops cell synthesis
   Gr +ve
   Gets exotoxin from virus via transduction
   Heart block
   Its toxoid therefore give antitoxin
   RSV (infants only)
   Mycoplasma
   Chlamydia pneumonia
   Strep pneumonia
   Mycoplasma
   Chlamydia pneumonia
   Strep. Pneumonia
   Strep pneumonia
   H. influenza
   Anaerobes
   Strep pneumonia
   Viruses
   Anaerobes
   H.influenza
   Gr –ve rods
   Monomer in blood
   Dimer in secretion
   Located on mucosal surface
   Found in secretion
   Only functions as surface marker for Mature B-
    Cell
   Immediate hypersensitivity/anaphylaxis
   Parasite defense
   Worms
   Fc region binds to mast cells and basophils
   Allergies
   Does Not fix complement
   Highest affinity
   Memory respond at day 3 five times the concentration
   Peaks in 5 years last for 10 years
   Opsonizes
   Activates complement
   2nd to show up in primary response
   Only one to show up for secondary respond
   Most abundant Ig in newborn
   Antigenic differences in heavy chain and site of di-
    sulfide bond
   4 subclasses G1 to G4
   Crosses placenta due to fc portion
   Most common sub-class deficiency
   Patient susceptible to encapsulated organisms
   Most memory antibody
   Only IgG NOT fixing complement
 Responds in primary response
 Most efficient in agglutination and complement
  fixation
 Defenses against bacteria and viruses
   MHC II
   IL-2
   IF- Gamma
   IL-4
   IL-5
   IL-6
   IL-10
   TH-1
   TH-2
   CD8
   CD8 becomes T-cytotoxic cells
   CD-3
   For what?
   Signal transduction

   CD-2
   For what?
   Adherence
   T helper cells
   T cytotoxic cells
   Myeloperoxidase
   NADPH
   Will kill ALL Gr+ve
     Ex..Hydrogen peroxide kills gr+
   Clue 4x7=28

   CD-4
   B-7
   CD-28
   Increased Chylomicron
   Deficiency of Lipoprotein lipase enzyme
   Defect in liver only
 Increased LDL
 Two types IIa and IIb
 Type IIa Receptor deficiency for LDL or missing
  B-100
 Type II-b (LDL and VLDL problems) enzyme
  deficiency for LDL at adipose. Receptor problem
  for VLDL. Most common in General Population
   Increased IDL
   Receptor problem for APO-E
   Increased VLDL
   Lipoprotein lipase enzyme deficiency at adipose
    tissue
   Combination of Types 1&4
   Increased Chylomicron and VLDL
   Enzyme and receptor deficiency at C-II
   Most common in diabetics
   Deposition of Cholesterol on elbows
   Can cause what?
   CAD
   Deposition of Triglycerides on eyelids, face
   Can cause what?
   Pancreatitis
   Little red spots w/ bright red margins
   Sandpapery
   RF- Jones critera
   Lymes disease
   Target lesions (bulls eye)
   Morbiliform rash
   Preceded by cough
   conjunctiivitis
   Fever x 2 day
   Followed by rash
   ONLY ONE WITH RASH FOLLOWING FEVER
    (HHV 6)
   Anterior aspect of leg
   Redness
   Tender nodules
   Red macules, target lesions
   Causes: allergy, viruses
   Mild: MCC virus, #2 drugs (sulfas)
   Moderate: Stevens-Johnsons Syndrome
   Severe: Toxic epidermal necrolysis , skin peels
    off
   Scaly skin with oily shine on headline
   Stuck on warts
   Due to aging
   HLA-B27
   Extensor surfaces
   Silvery white plaques
   Scaly skin
   Pitted nails
   STAGES
   Red macules
   Papules
   Vesicles
   Pustules then scabs
   Different stages may appear at same time
   Rash and blisters on ant. thighs
   Assoc. with diarrhea
   Assoc. with flare up of celiac sprue
   SEEN WITH SALMONEALLA INFXN
   Rose spots assoc. with intestinal fire
   Heliotropic rash
   Reddened area on skin w/ raised borders
   DOES NOT BLANCH
   Redness
   Itchy groin
 Herald patch= dry skin patches that follow skin
  lines
 HHV 7
   Hypopigmented macules on upper back
   Presents in a V pattern
   A.K.A. upside down christmas tree
   Tx: Griseofulvin
   Linear excoriations on belt line and finger webs
   What is the tx?
   Lindane
   Permethrin
   DiGeorges
   What ion imbalance will they have?
   Hypokalemia
   What did not form?
   3rd and 4th pharyngeal pouch
   What chromosome?
   Deletion on chromosome 22
   HIV
   Also B-cell but less so
   NOT A FUNGUS
   Non-Hodgkins form of cutaneous T-cell
    lymphoma
   Transport TG’s from GI to liver and endothelium
   Transports TG’s from liver to adipose
   Transports TG’s from adipose to tissue
   ONLY ONE THAT CARRIES CHOLESTEROL
   XANTHELASMA

   Where are they located?
   On eyelids and eyebrows
   Xanthomas

   Where are they located?
   elbows
   ONLY ONE MADE IN THE LIVER
   ARE BREAK DOWN PRODUCTS OF VLDL
   Gram -/+?
   Pleomorphic gram (-) rods
   What pattern?
   “school of fish pattern”
   What type is most common?
   Type A
     80%
   Capsule or no capsule?
   non-encapsulated
   Invasive or non invasive?
   non-invasive
   Most common cause of what?
   Sinusitis
   Otitis
   Bronchitis
   What is the 2nd most common type?
   TYPE B
     20%
   Encapsulated or non encapsulated?
   Encapsulated
   What does it have in its capsule?
   Polyribosyl phosphate in capsule
   Contains IgA protease
   Invasive or non invasive?
   Invasive
   What does it cause most often?
   #1 cause of epiglottitis
   What are the signs of epiglottitis?
   Stridor
   Fever
   Thumb sign on xray
   0-2 months?
   #1. Group B strep (agalactiae)
   #2. E. coli
   #3. Listera
   2 Months- 10 years?
   #1. strep pneumonia
   #2. n. meningitides
   (adolescent years only)
   10yrs- 21 yrs?
   #1. n. meningitides
   > 21 years old?
   #1 S. pneumoniae
   At what age is it given?
   Given at 2,4,6 months
   What strain does it cover?
   Covers 23 strains (98% cases)
   Indications?
   Anyone> 65y/o
   Anyone splenectomized
     Sickle cell anemia
   Anyone with end-organ damage
     CF
     RF
     Nephrotic Syndrome
   MCC of all throat infections
   #2 MCC of all what?
   Skin infections except lines
   St. aureus?
   Gold pigment
   St. epidermidis?
   White pigment
   St. saprophyticus?
   No pigment
   Strep. Pneumonia
     pneumococcus
   Skin Infections?
   Say Staph. Aureus

   Throat Infections?
   Say Strep. Pyogenes

   Small Intestine Infections?
   Say E. coli
   Job Syndrome:
   IL-4
   Hyper IgE
   What do they look like?
   Red hair
   Fair complexion
   Female
   NADPH-OXIDASE DEF (CGD)
   NEUTROPENIA
   MYLOPEROXIDASE
   Job-Buckley Syndrome
   HbC antigen
   HbS antigen
   HbC antigen
   HbS antigen
   HbC antibody
   HbS antigen ONLY
   HbS antibody ONLY
   HbC antibody
   HbS antibody
   HbS antigen
   IgG
   HbS antigen for >6months
   Can be with or without HbS antibody
   HbE antigen
   HbE antibody
   NEGATIVE HbS antigen
   POSITIVE HbS antigen
   HbE antibody
   IgM HbC antibody

   What disappears?
   HbS antigen
   4 to 26 wks
   Average @ 8wks
   4 to 12 wks
   4 to 20 wks
   YEARS
   MC infection?
   CMV
   MCC of death?
   PCP
   What is p41 used for?
   Just a marker
   What does Gp120 do?
   Attachment to CD4
   What is Pol used for?
   Integration
   What is reverse transcriptase used for?
   Transcription
   What are p17 & p24 antigens used for?
   Assembly
 What is the normal CD4 count?
 800-1200
 What can the CD4 count be up to in children?
 1500
 When do you begin treating with 2 nucleotide
  inhibitors and 1 protease inhibitor?
 <500
     (child at 750)
   AIDS is defined as a CD4 count of what?
   <200
   With a CD4 count of <200 what do you tx for?
   PCP
   What do you treat for when CD count is <100?
   Mycobacterium aviam intracellular
   Vitamin E
     #1
   Vitamin A
   Vitamin C
   Betakertine
   Parathyroid

   Along with what other cofactor?
   Mg+
   Hyperparathyroid
     Increase Ca+
     Decrease Phosphate
   What will be the symptoms?
   Goans
   Moans
   Bones
   Stones
   Pseudotumor Cerebri
     Increase CSF production from Chorichoid Plexus
   Pseucotumor cerebri
   Nightvision problems/nightblindness

   Hypoparathyroidism
     Decrease Ca+
     Increase Phosphate
   THIAMINE

   What do you get with a decrease in thiamine?
   Beri Beri

   What is the most common cause in US?
   ETOH
   Wet Berry Berry
   With heart failure

   Dry Berry Berry
   Without heart failure
   Wernicke’s Encephalopathy

   Wernicke’s Korsakoff
   Alcoholic thymine deficiency of the Temporal
    Lobe
   3 Dehydrogenases
   Pyruvate dehydrogenase
   Alpha ketoglutarate dehydrogenase
   Branch chain amino acid dehydrogenase

   Transketolase
   Riboflavin

   What is a physical sign of this deficiency?
   Angular stomatitis
   Angular cheliosis
   Corneal Neurovasculazations
   Milk
   Also from FAD
   Niacin

   What is the clue?
   Diarrhea
   Dermatitis
   Dementia
   Death
   Hartnup Disease

   What is deficient in this disease?
   Tyrptophan

   What is typtophan needed for?
   Needed for niacin formation
   Lipoic acid

   What is the deficiency caused by this vitamin?
   Not one
   Pantothenic acid

   What is the deficiency caused by this vitamin?
   You guessed it…nothing
   Pyridoxine

   What is the deficiency caused by this vitamin?
   Neuropathy
   Seizures

   Who do you need to give B6 to?
   Patient on INH
   Sideroblastic
   ALL transaminases
   Cyanocobalamine

   What is the deficiency caused by this vitamin?
   Pernicious anemia
   Neuropathy
   Pernicious anemia
   Methylmalonyl CoA Mutase
   Homocysteine Methyl Transferase
   Neuropathy

   Why?
   Because it recycles myelin
   Megaloblastic anemia

   What else is this enzyme needed for?
   Nucleotide synthesis
   VITAMIN B2- RIBOFLAVIN deficiency
   DIARRHEA
   DERMATITIS
   DEMENTIA
   DEATH
   PYRIDOXINE B6
   B12 CYANOCOBALAMINE
   Folate
   Megaloblastic anemia

   With neuropathy?
   NO NEUROPHATHY

   What else is Folate used for?
   Nucleotide synthase (THF)
   Ascorbate acid
   Collagen synthesis
   Scurvy
   Bleeding gums
   Bleeding hair follicles
   Diet deficient in citrus fruit
   Diet deficient in green vegetables
   Over cooked green vegetables
   Controls Ca+
   Absorbes Ca+ from GI
   Reabsorbs Ca+ in Kidneys

   Controls osteoblastic activity
   Ricketts

   What does it cause in ADULTS?
   Osteomalcia
   Lateral Bowing of the Legs
   X-linked dominant
   Hair
   Skin
   Eyes
   Protection against free radicals
   #1 antioxidant
   Retinopathy
   Folate
   Vitamin K
     90%
   Biotin
   Panothenic acid
   Helps with absorption of B12
   1972
   Protein C
   Protein S
   Which one has the shortest half-life?
   Protein C
   Which one has the 2nd shortest half-life?
   7
   Chromium
   Selenium
   Manganese Molebdenum
   Tin
   Insulin action
   Heart
   Manganese Molebdenum
   Hair
   Dysguzia
   Decrease sperm
   Dry hair
   Dry skin
   Mg+
   Biotin
   Pyridoxine
     B6
   ALL carboxylases
   ALL kinases
   Parathyroid along with Vitamin A
   Muscle contraction
   Axonal transport
   2nd messengers
   Dorsal Columns
   Cortical Spinal Tracts

   Why are these affected?
   Because they are the longest
   Because they need the most myelin
   Maganese Molebdenum
   By the liver
   Always Hepatotoxic
   By the kidney
   Always nephrotoxic
   Pain
   Pallor
   Paresthesia
   Pulselessness
   Poikilothermia
   Lympangitis
   Impetigo (not bullous)
   Necrotizing fascitis
   Erysepelas
   Scarlet fever
   Lympangitis
   Impetigo (not bullous)
   Necrotizing fascitis
   Erysepelas
   Scarlet fever
   Staph epidermitis
   Staph aureus
   Absorption of Vit. B12
   Synthesis of:
     -Vitamin K
     -Biotin
     -Folate
     -Pantothenic acid
       ▪ B5
   Trypsin cuts where?
   cuts to R of
   Arg
   Lys
   Chymotrypsin cuts where?
   cuts to R of bulky aa’s (aromatics)
   Phe
   Tyr
   Trp
   Elastase cuts where?
   Cuts to R of (“SAG”)
   Ser
   Ala
   Gly

   CNBr cuts where?
   Cuts to R of
   Methionine
   Aminopeptidase cuts where?
   Cuts to R of
   amino acid terminal

   Caboxypeptidase cuts where?
   Cuts to L of
   carboxy terminal
   MMR
   MMR & INFLUENZA
   Hepatitis B
   Hib
   Diphtheria
   Pertussis
   Strain 12
   Myeloperoxidase
   NADPH Oxidase
   NADPH Oxidase

   Which means they only kill what?
   Kills only G -ve
   IL-1
   IL-6??
   DDI>DDC
   Pancreatitis
   Leigh’s Disease
   What is another name?
   Subacute necrotizing encephalomyelopathy
   What are the signs & symptoms?
   Progressively decreasing IQ
   Seizure
   Ataxia
   What is the deficiency?
   Cytochrome oxidase deficiency
   Leber’s Hereditary Optic Atrophy (LHON)
   They all die
 Listeria

   What part is toxic?
   Lipid A

   Does it cross the placenta?
   Yes
   T-cells & Macrophages, therefore, have
    granulomas
   Raw cabbage
   Spoiled milk
   Migrant workers
   Birth – 2 months
   4 – 7 years old
   Puberty
   DiGeorge’s Syndrome
   Lysine
   Arginine
   Glutamate
   Aspartate
   Phenylalanine
   Isoleucine
   Trptophan
   Threonine
   Phenylalanin
   Tyrosine
   Tryptophan
   Met
   Cyst
   Proline
   Gly
   Serine
   Threonine
   Tyrosine
   Asparagine
   Glutamine
   Leu
   Iso
   Val
   Leu
   Lys
   Psoriasis (with arthritis)
   Ankylosing Spondylitis
   Irritable Bowel Syndrome
   Reiter’s Syndrome
   Psoriasis with out arthritis
   Strep. Pneumoniae
   H. influenza
   Neisseria catarrhalis
   Histaminase
   Arylsulfatase
   Heparin
   Major Basic Protein
   In an Acute Reaction?
   Histamine

   In a Late Reaction   ?
   SRS-A
   ECF-A
   0 – 2 months?
   chlamydia pneumonia
   Intersitital pneumonia
   High temperature with NORMAL pulse rate!

(This should never be! Each degree ↑ in temp. → 10
  beats/min ↑ in pulse rate)
 FEVER
 NONSPECIFIC ILLNESS
 RECRUITS TH CELLS for LINKING with MHC II
  COMPLEX
 SECRETED BY MACROPHAGES
 MOST POTENT OF THE Interleukins
 RECRUITS EVERYBODY
 MOST POWERFUL CHEMO-ATTRACTANT
 MUST BE INACTIVATED
 When must you inactivate it?
 PRIOR TO TRANSPLANTATION
  by cyclosporin
 SECRETED BY TH1 CELLS
 ENERGIZED MACROPHAGES
 CAUSES B-CELL PROLIFERATION
 LABELED BY THYMIDINE (USE POKEWEED
  MITOGEN OR ENDOTOXIN)
 SECRETED BY ACTIVATED T CELLS
   B-CELL DIFFERENTIATION
   RESPONSIBLE FOR CLASS SWITCHING
   SECRETED BY TH2 CELLS
   They do exactly what IL-1 thru IL4
 SUPPRESSES CELL-MEDIATED RESPONSE (tells
  macrophages and fibroblasts to stay away if
  bacterial)
 INHIBITS MAC ACTIVATION
 PROMOTES CELL-MEDIATED RESPONSE
  (recruits macs & fibroblasts if NOT bacterial)
 ACTIVATES NK CELLS TO SECRETE IF-γ
 INHIBITS IL-4 INDUCED IgE SECRETION
 CHANGES TH CELLS to TH1 CELLS
     secretes IL-2 & IF-γ → inhib. TH2, therefore, ↑ host
      defenses against delayed hypersensitivity
   Where is it from?
   LEUKOCYTES
   ↓VIRAL REPLICATION AND TUMOR GROWTH
   ↑ NK ACTVITY
     secretes perforins and granzymes to kill infected cell
   ↑MHC CLASS I & II EXPRESSION
   ↓ PROTEIN SYNTHESIS
     translation inhibited, therefore, defective protein
      synthesis
   Increase NK activity
   Increase MHC class I & II
   Decrease protein synthesis
   Decrease viral replication and growth
   Where is it from?
    FIBROBLASTS
   Increase NK activity
   Increase MHC class I & II
   Decrease protein synthesis
   Decrease viral replication and growth
 Where is it from?
 T-CELLS & NK CELLS
 ↑ NK ACTIVITY
 ↑MHC CLASS I & II
 ↑ MACROPHAGE ACTIVITY
 CO-STIMULATES B-CELL GROWTH &
  DIFFERENTIATION
 ↓ IgE SECRETION
   Where is it from?
   MONOCYTES & MACROPHAGES
   What is another name for TNF-alpha?
   CACHECTIN
   INDUCES IL-1
   ↑ ADHESION MOLECULES & MHC CLASS I ON
    ENDOTHELIAL CELLS
   PYROGEN
   INDUCES IF-γ SECRETION
   CYTOTOXIC/CYTOSTATIC EFFECT
   Where is it from?
   T-CELLS

   What is another name for it?
   LYMPHOTOXIN

   CYTOTOXIC FACTOR
   Where is it from?
   SOLID TUMORS (CARCINOMA > SARCOMA)
   MONOCYTES

   What is another name for it?
   TRANSFORMING GROWTH FACTORS
   What does it INDUCE?
   ANGIOGENESIS
   KERATINOCYTE PROLIFERATION
   BONE RESORPTION
   TUMOR GROWTH

   What is it mainly for?
   MAINLY FOR TUMOR GROWTH
   Where is it from?
   PLATELETS
   PLACENTA
   KIDNEY
   BONE
   T & B CELLS
   What INDUCES it?
   FIBROBLAST PROLIFERATION
   COLLAGEN
   FIBRONECTIN SYNTHESIS
   What INHIBITS it?
   NK
   LAK
   CTL
   T & B CELL PROLIFERATION
   What ENHANCES it?
   WOUND HEALING
   ANGIOGENESIS
   What does it suppress?
   SUPPRESSES IR AFTER INFECTION &
    PROMOTES HEALING PROCESS

   What is it mainly for?
   MAINLY FOR WOUND HEALING
   LYMPHOKINE ACTIVATED KILLER CELLS
   CYTOTOXIC T-LYMPHOCYTES
   CNS
   Heart
   Skeletal muscle

   Why does it affect these particular places?
   Due to uneven cytokinesis during meiosis or
    oogenesis
   Who are affected?
   All offspring

   Who passes the disease?
   MOM

   Who has no transmission?
   Dad
   Who does it show in?
   Not parents
   Siblings/uncles may show disease
   When is onset?
   Early in life (childhood diagnosis)
   Is it complete on incomplete penetrance?
   COMPLETE
   How are they acquired?
   Almost ALL are inborn error of metabolism

   When does it occur?
   Only when both alleles at a locus are mutant
   How is it transmitted?
   Horizontal Tm

   Are there malformations present?
   Physical malformations are uncommon

   What type of defect?
   Enzyme defect
   Who does it affect the most?
   M=F

   How does it manifest?
   Heterozygote state

   Who can transmit the disease?
   Both parents
   Where is the new mutation?
   Often in germ cells of older fathers

   When is onset?
   Often delayed (adult diagnosis)
     Example = Huntington’s
   What is penetrance?
   Reduced penetrance

   How is it expressed?
   Variable expressin
     Different in each individual
   How is it transmitted?
   Vertical TM

   Is there malformation present?
   Physical malformation common

   What type of defect?
   Structural
   Maternal grandfather
   Maternal uncle
   What happens <24hrs?
   Swelling

   What happens at 24 hrs?
   Neutrophils show up

   What happens at day 3?
   Neutrophils peak
   What happens at day 4?
   T cells and Macrophages show up

   What happens at day 7?
   Fibroblasts show up

   What happens in 1 month?
   Fibroblast peak
   What happens at 3-6 months?
   Fibroblasts are gone
   Lysosomal Inclusion Bodies
   Gauchers
   Fabrys
   Krabbe
   Tay Sachs
   Sandhoffs
   Hurlers
   Hunters
   Neiman Pick
   Metachromatic Leukodystropy
   Beta-Glucocerberosidase

   What Accumulates?
   Glucocebroside

   Where?
   Brain
   Liver
   Bone Marrow
   Spleen
   Ask. Jew
   Gargols
   Gaucher cells
     Macrophages looking like Crinkeled paper
   Erlin myoflask legs
   Pseudohypertrophy
   Alpha-galactosidase

   What accumulates?
   Ceramide Trihexoside
   X-Linked recessive
   Presents with cataracts as a child
   Presents with renal failure as a child
   Galactosylceramide B-Galactosidase

   What accumulates?
   Galactocerebrosidase

   Where?
   Brain
   Early death
   Globoid bodies
     Fat cells
   Hexoseaminidase A

   What accumulates?
   GM2 Ganglioside
   Ask. Jews
   Cherry red macula
   Death by 3
   Hexoseaminadase A & B
   Iduronidase
   Corneal Clouding
   Mental Retardation
   Iduronate Sulfatase
   Mild mental retardation
   No corneal clouding
   Mild form of Hurlers
   X-linked recessive
   Spingomyelinase

   What accumulates?
   Spingomyelin
   Cholesterol
   Zebra bodies
   Cherrry red macula
   Die by 3
   Arylsulfatase A
   Visual Disturbance
   Presents like MS in 5 to 10 years of age
   Von Gierkes
   Andersons
   Corys
   McCardles
   Pompes
   Hers
   G-6-Pase Deficiency
   Big Liver
   Big Kidney
   Severe hypoglycemia
   Can NEVER raise their blood sugar
   Branching enzyme deficiency
   Glycogen will be ALL LONG chains on liver
    biopsy
   Debranching enzyme
   Glycogen from liver biopsy will be ALL SHORT
    branches
   Muscle phosporalase
   Severe muscle cramps when exercising
   High CPK
   Cardiac alpha-1,4 glucocydase
   Heart problems
   Die early
   Liver phosphoralase
   Big Liver
   NO big kidney
   Intraductal Ca
   AV Fistula
   Vasodilation
   Tay Sachs
   Sandhoffs
   Niemann Pick
   CML
   Ewing’s sarcoma
   Burketts lymphoma
   Follicular lymphoma
   Sarcoid
   Amyloid
   Hemochromatosis
   Cancer
   Fibrosis

   Thanks STAN!!
   Shistocytes
     Burr cells
     Helmet cells
   Splenomagely
   Adrenal
   Liver
   G6PD
   Lead poisoning
   Iron deficiency
   Anemia of Chronic disease
   Lead poisoning
   Hemoglobinopathy
   Thallasemia’s
   Sideroblastic anemia
   Genetic
   AD
   Blood transfusions
   Hereditary Spherocytosis
   Acute hemorrhage
   Anemia of Chronic Disease
   Hypothyrodism
     Early
   Renal Failure
   Folate deficiency
   B12 deficiency
   Reticulocytosis
   ETOH
   Hemolytic Anemias
   Chemo Treatment
   Anticonvulsants
   Myelodysplasia
   Phenytoin
   Ethusuximide
   Carbamyazapine
   Valproate
   Sideroblastic anemia
   Something is wrong with the RBC membrane
     Extravascular
   Heridatary Ellitocytosis
   Increased RET count
   Wilson’s Disease
   Hepato/Lenticular Degeneration
   Kayser Fleishner Rings
     Copper in eyes


   Hepato = Liver
   Lenticular = Movement problem
   Collagen synthesis
   Minky Kinky Hair Syndrome
   Epinephrine
   Norepinephrine
   Dopamine
   Tyrosine
   Adrenal Pheochromocytoma
   Blocks DNA gyrase (topoisomerase II)
   Inhibits p450
   All Gram + including staph auerus
   All Gram –
   Atypicals
   Chlamydia
   Ureoplasma
   Mycoplasma
   Legionella
   Cortisol
   Epinephrine
   Glucagon
   Glycosaminoglycan chain that helps form
    proteoglycans
   Glycosaminoglycan chain that helps form
    proteoglycans
   Inhibits dihydrofolate reductase
   Inhibits DNA synthesis in the S phase of cycle.
   Prevents reduction of folic acid needed to
    produce THF
   Purine nucleotide synthesis
   Methylation of dUMP to for dTMP
   Obstructs one carbon methylation which
    deprives DNA polymerase of essential substrates
   CF
   Galactosemia
   Defects in Glycolysis
   Defects in Hexose Monophosphate Shunt
   B12
   B12
   Vitamin B6
   Vitamin C
   Occurs in the synthesis of Blood Clotting factors
   Requires Vitamin K
   Thiamine
   Vitamin D
   Vitamin A
   Thiamine
   Olfactory
   What is its function?
   Sensory for smell
   What if lesioned?
   Anosmia
   Where does it Exit/Enter the Cranium?
   Cribriform plate
   What does it innervate?
   Nasal Cavity
   Optic
   What is its function?
   Sensory for sight
   What if lesioned?
   Anopsia
     Visual field defect
   Loss of light reflex with CN III
   Only nerve affected by MS
   Where does it Exit/Enter the Cranium?
   Optic Canal

   What does it innervate?
   Orbit
   Occulomotor
   What are the functions?
   Motor
   Moves the eyeball in ALL directions
   Adduction Most important action (MR)
   Constricts the pupil (Spincter Pupillae)
   Accomodates (Cililary Muscle)
   Raises eyelid (Levator Palpebrae)
   What if lesioned?
   Diplopia
   Loss of parallel gaze
   Dilated pupil
   Loss of light reflex
   Loss of near response
   Ptosis
   Where does it Exit/Enter the Cranium?
   Superior Orbital Fissure

   What does it innervate?
   Orbit
   Trochlear
   What is its function?
   Motor
   Superior Oblique
   Depresses and abducts the eyeballs
   Intorts
   What if lesioned?
   Weakness looking down w/ adducted eye
   Trouble going down stairs
   Head tilts away from lesioned side

   Where does it Exit/Enter the Cranium?
   Superior Orbital Fissure
   What does it innervate?
   Orbit
   Trigeminal
   V1?
   Opthalmic

   V2?
   Maxillary

   V3?
   Mandibular
   Mixed
   General sensation (touch, pain, temperature) of the
    forehead, scalp, & cornea
   What if lesioned?
   Loss of general sensation of the forehead/scalp
   Loss of blink reflex w/ VII
   Where does it Exit/Enter the Cranium?
   Superior orbital Fissure
     Ophthalmic division
   What does it innervate?
   Orbit
   Scalp
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Step 1 Clues 1135 Slides

  • 1.
  • 2. Huntington’s  Fragile X  Myotonic Dystrophy  Prader Willie  Spinal/bulbar muscular atrophy (Fredicks ataxia)
  • 3. Aortic Arch  Upper Esophagus  True Vocal Cords
  • 4. Cilia
  • 5. •Myositis •1 muscle hurts •Polymyocytis •Bunch of muscles Hurt •Dermatomyositis •HELIOTROPIC RASH + muscle pain •Fibrositis •Muscle insertions hurt when you move them •Fibromyalgia •Hurts all the time •Polymyalgia Rheumatica •Weekness in the SHOULDER GURDLE…. Associated with temporal arteritis •Temporal Arteritis •Macrophages eating temporal artery, ESR > 60
  • 6. RIPS  Rifampin  INH  Predinsone  -Statins
  • 7. Hypothyroidism (Hashimoto)  Cushing disease
  • 8. T. Spiralis
  • 9. Arylsulfatase deficiency  Metachromatic leukodystoryphy
  • 10. G6-PD  CGD  Pyruvate dehydrogenase Def.  Fabry’s  Hunter’s  Lesch-nyhan
  • 11. Decreased Protein  WHY? ▪ Decreased intake ▪ Cirrhosis ▪ Nephrotic Syndrome ▪ Merrentic Syndrome
  • 12. Kidneys ( at all times )
  • 13. Diabetes Mellitus
  • 14. Riley-Day Syndrome
  • 15. Shy-Dragger Syndrome  CLUES? ▪ Pt. gets up and passes out
  • 16. Sick Sinus Syndrome
  • 17. Pituitary adenoma  White nipple discharge = most likely milk due to increased prolactin
  • 18. Ileum
  • 19. Sigmoid Colon
  • 20. Choanal atrasia  Turning blue on breast feeding  C-Type Esophageal Atresia  Duodenal Atresia  Down syndrome  Double bubble sign
  • 21. Pyloric stenosis
  • 22. Achalasia
  • 23. Intussuseption  CLUES ▪ Knees in chest ▪ Sausage shaped mass ▪ Current jelly Stool
  • 24. Adhesions  Internal Hernias
  • 25. Hirschsprung’s Disease
  • 26. Adhesions
  • 27. Adhesions  Obstruction  Cannot move stool  Diverticulitis  Cancer
  • 28. Mesonephrons
  • 29. Reticulonodular appearance  May progress to Honey comb lung  Gradual onset dyspnea, first evident only on exertion
  • 30. OA  Septic Artheritis  Crystal induced(GOUT)
  • 31. RA  Viral  SLE
  • 32. Ankylosing spondylitis
  • 33. Gonoccal Artheritis  Rheumatic Fever  Lyme Disease
  • 34. LH  FSH  TSH
  • 35. DM type 2  Niacin  HPL ( Human Placental Lactogen )
  • 36. Acanthosis Nigracan
  • 37. Because of the LIVER
  • 38. Polyhydramnios
  • 39. Reily Day Syndrome  Baby cries but no tears  Werdnig Hoffmann disease  Fasciculation is a newborn
  • 40. Oligohydramnios
  • 41. CC LL S  Chagas Disease (Whipple’s)  C. Diptheria  Lyme Disease  Legionella  Salmonella typhii (typhoid)
  • 42. CC S Y  Crohn’s  Chlamydia  Shigella  Yersina
  • 43. I AM HE  Influenzae  Adenovirus  Mycoplasma  Hepatitis C  EBV
  • 44. H I PPPE  Hydralazine  INH  Phenytoin  Procainamide  Penicillamine  Ethosuximide
  • 45. ABC V  AZT  Benzene  Chloramphenicol  Vinblastine  Vinblastine Anilate Bone Cells
  • 46. Vibrio  Campylobacter  Listeria  H. pylori  Campylobacter Has Very Long Comma Genes
  • 47. Giardia lamblia
  • 48. Corynebacterium Diptheria  CLUES ▪ Grey membrane ▪ Inhibits EF-2
  • 49. RESPI  Rifampin  Ethambutanol  Streptomycin  Pyrazinamide  INH
  • 50. C SSS PM  Cryoglobinemia (I AM HE)  Serum Sickness (Type III hypersen.)  SLE ( ANA, Anti-ds-DNA, Anti-Smith)  SBE ( new onset murmur )  PSGN ( RBC cast )  MPGN II ( NFe3)
  • 51. C (SEE) ! QT(CUTIE) BRAGS because she can induce p450  Carbamazapine  Quinidine  Tetracycline  Barbiturates  Rifampin  Alcohol  Griseofulvin  Sulfa drugs
  • 52. I Do SMACK  INH Quinolones  Dapsone  Spirolactones  Macrolides  Amiodarone  Cimetidine  Ketoconazole  Quinilones
  • 53. WET DumP  Warfarin  Estrogen  Theophylline  Digoxin  u  m  Phenytoin
  • 54. CGD
  • 55. Chronic Granulomatous disease  NADPH Oxidase deficiency
  • 56. Myositis  Hepatitis  Increased liver enzymes
  • 57. Chancroid  Herpes  Lymphogranuloma inguinale
  • 58. Haemophilus ducreyi
  • 59. Cystine  Methionine
  • 60. Mercaptoethanol
  • 61. PI IG (pig)  Prolactin  Insulin  Inhibin  GH
  • 62. PI IG (pig)  Prolactin  Insulin  Inhibin  GH  Because Cystine makes disulfide bonds
  • 63. Mercaptoethanol cuts where?  Cuts to R of: disulfide bonds  Cysteine  methionine
  • 64. CLAM  Chloramphenicol  Lactams  Cefamandole  Cefoperazone  Antabuse  disulfiram  Metronidazole
  • 65. When do you see elevated ESR?  Non-specific inflammation  When do you see Falsely high ESR?  Anemia  When do you see Falsely LOW ESR?  Sickle Cell Anemia  Polycythemia  Acute Phase Reactants?  IL-6
  • 66. Amyloidosis
  • 67. AA  Acute inflammatory Disease  AB  Alzhiemer’s Disease  AB-2  Chronic Renal Failure  AE and AF  MEN – II  AL  Multiple Myeloma
  • 68. Fibroblasts  Simple scarring  Myofibroblasts  Wound contraction
  • 69. NEAT ASs Hooks  Necatur americanis  Enterobius vermicularis  Ankylostoma duodenale  Trichuris trichurium  Ascaris lumbercoides  Strongyloides
  • 70. Please  PKU  Check  CAH(Congential Adrenal Hyperplasia)  Before  Biotinidase  Going  Galactosemia  Home  Hypothyroidism
  • 71. HLA-DR2 ▪ Narcolepsy ▪ Allergy ▪ Goodpasture’s ▪ MS  HLA-DR3 ( CC D SS ) ▪ Celiac Sprue ▪ Chronic Active Hepatitis ▪ DM, ▪ Sjogren’s, ▪ SLE,  HLA-DR3 & 4  IDDM(Type I)
  • 72.  HLA-DR4  Rheumatoid Arthritis,  Pemphigus Vulgaris  HLA-DR5  JRA  Pernicious Anemia  HLA-DR7  Nephrotic Syndrome(Steroid induced)
  • 73. HLA-DR 3 & B8  Celiac Disease  HLA-A3  Hemochromatosis ▪ (ch 6, point mut.- cysteine > tyrosine)  HLA-B8  MG  HLA-B13  Psoriasis
  • 74. HLA-B27= (PAIR)  Psoriais(only if w/arthritis)  Postgonococcal Arthritis  Ankylosing Spondylitis,  IBD,  Reiter’s,  HLA-BW 47=  21 alpha Hydroxylas def.(Vit.D)
  • 75. Kills helper T-cells & eosinophils  Inhibits Macrophage migration  Inhibits Mast cell degranulation  Inhibits Phospholipase A  Stimulates protein synthesis  Stablizes endothelium
  • 76. STELS  Salmonella (typhoid)  TB  EBV  Listeria  Syphillis
  • 77. UTI  Spontaneous bacterial peritonitis  Abdominal abscess  Cholecystitis  Ascending cholangitis  Appendicitis
  • 78. Ceftriaxone  Cefixime  Cefoxine  Ciprofloxin  Oflaxacin  Gatifolxacin
  • 79. Azithromycin
  • 80. Strep bovis  Clostridium melanogosepticus  Bacteriodes fragilis
  • 81. Clindamycin  Metranidazole  Cefoxitin
  • 82. Strep. Bovis  Clostridium melanogosepticus
  • 83. K+?  Decreases  Na+?  Decreases  Cl-?  Decreases  pH?  Increases  BP?  Increases
  • 84. Calcified CA’s
  • 85. PSAMMoma bodies  Papillary carcinoma of the Thyroid  Serous cyst Adenocarcinoma of the ovary  Meningioma  Mesothelioma
  • 86. P PUNCH  Proteus  Pseudomonas  Ureaplasma urealyticum  Nocardia species  Cryptococcus neoformans  H. pylori
  • 87. Struvite (90%)
  • 88. swarming
  • 89. Brain  Microglia  Lungs  Type I Pneumocytes  Liver  Kuffler cells  Spleen  Reticuloendothelial Cells (RES Cells)  Peyer’s patch  M-Cells  Blood  Monocytes
  • 90. Kidney  Mesangal Cells  Bone  Osteoclast  Lymph Node  Dendritic Cells  Skin  Langerhan Cells  Connective tissue  Epithelioid  Giant cells  Histiocyte
  • 91. Intractable pain  Hemorrhage (massive)  Obstruction (from scarring)  Perforation
  • 92. Adriamycin (Doxyrubicin)  Phen-fen
  • 93. Dozaroxsin
  • 94. #1 = Virus  #2 = Drugs
  • 95. High Fever  Rose spots (rash)  Intestinal fire
  • 96.  Some  *Strep. Pneumo (gr+) MC  Strange  Salmonella  Killers  Klebsiella  Have  Pretty  H. influenza  Nice  Pseudomonas  Capsules  Neisseria  Cryptococcus
  • 97. Spleen  Think!!! splenectomy pt. with infections
  • 98. SubQ nodules  Polyarthritis  Erythema marginatum  Carditis  Chorea
  • 99. Neoplasms  Allergies/Asthma  Addison’s Dz  Collagen Vascular Dz  Parasites
  • 100. B.S HAVE CASH  Benzene  Schistomiasis  Hep B,C,D  Aflatoxin  Vinyl chloride  Ethanol  Carbon Tetrachloride  Anyline Dyes  Smoking  Hemochromatosis
  • 101. MMR OR SBYV  Measles  Mumps  Rubella  Oral Polio (sabin)  Rotavirus  Small pox  BCG  Yellow fever  Varicella
  • 102. RIP Always  Rubella  Influenza  Polio ( salK ) [Killed]  HAV
  • 103. Henoch-Schoenlein P. (HSP)  Alport’s  Berger’s
  • 104. PCN  α-methyldopa  Cephalosporins  Sulfa  PTU  Anti-malarials  Dapsone
  • 105. ASA  Heparin  Quinidine
  • 106. T CAL  Troponin I  CKMB  AST  LDH flip
  • 107. T CAL  Troponin I  Appears  2 hrs  Peaks  2 days  Gone  7 days
  • 108. T CAL  CK-MB  Appears  6 hrs  6 x 1 =6  Peaks  12 hrs  6 x 2 = 12  Gone  24 hrs  12 x 2 = 24
  • 109. T CAL  LDH1  Appears  1 day  Peaks  2 days  Gone  3 days
  • 110.
  • 111. HUMORAL  CELL MEDIATED  Blood sample  Tissue sample ( BIOPSY)  B-Cells &  T-Cells and Macrophages Eosinophils/neutrophils  TH-1  TH-2  Inhibited by IL-10  Inhibited by INF-Gamma  EVERYTHING ELSE  ALL BACTERIA ▪ Virus (#1 .CMV, #2. EBV) ▪ Fungus ▪ Micobaterium ▪ Protozoa ▪ Parasite ▪ neoplasm
  • 112. Brain  Microglia  Lungs  Type I Pneumocytes  Liver  Kuffler cells  Spleen  Reticuloendothelial Cells (RES Cells)  Peyer’s patch  M-Cells  Blood  Monocytes
  • 113. Kidney  Mesangal Cells  Bone  Osteoclast  Lymph Node  Dendritic Cells  Skin  Langerhan Cells  Connective tissue  Epithelioid  Giant cells  Histiocyte
  • 115. Legionella  Pneumocysitis carinii  H. pylori  Bartonella henseslae (lymph node)  Candida (yeast)
  • 116. Sulfonamides  Sulfonylurea  Celebrex
  • 117. *Celecoxib
  • 118. COX 2 specific
  • 119. Vioxx (Rofecoxib)
  • 120. Pyremethamin/Sulfadiazine  Trimethoprim/Sulfamethoxazole
  • 121. Bleomycin  Bulsufan  Amiodarone  Tocainide
  • 122. Chediak-Higashi  NADPH-oxidase deficiency
  • 123. Hyperglycemia  Hyperuricemia  Hypovolemia  Hypokalemia
  • 124. OH DANG  Ototoxicity  Hypokalemia  Dehydration  Allergy  Nephritis (interstitial)  Gout
  • 125. MR  Decrease on inspiration (^exp)  TR  Increase on inspiration  VSD  Decrease on inspiration (^exp)
  • 126. Brain  Mircoglia  Lung  Type I pneumocyte  Liver  Kupffer cell  Spleen  RES  Kidney  Mesangial  Lymph nodes  Dendritic  Skin  Langerhans  Bone  Osteoclasts  CT  Histiocytes or  Giant cells or  Epithelioid cells
  • 127. RC KT SSS  Rocky Mountain Spotted Fever  Coxsackie A (Hand/Foot & mouth dz)  Kawasaki  TSS  Syphillis  Scarlet Fever  Staph Scalded Skin Syndrome
  • 128. Tachypnea  Decrease pCO2  Decrease pO2  Increase pH
  • 129. cAMP  cGMP  IP3/DAG  Ca:Calmodulin  Ca+  Tyrosine kinase  NO
  • 130. It is the 90%  Sympathetic  CRH (cortisol)  Catabolic
  • 131. Parasympathetic  Anabolic
  • 132. Neurotransmitter  GHRH  All hypothalamic hormones xc cortisol  Used by what and for what? ▪ Smooth muscle for contraction
  • 133. Used by smooth muscle for contraction by distention
  • 134. Used by Gastrin only
  • 135. Used by Insulins  Used by ALL growth factors
  • 136. Nitrates  Viagra  ANP  LPS
  • 137. AR  Defect in LFA-1 integrin proteins on phagocytes  Absent pus formation  Delayed separation of umbilicus  Recurrent bacterial infections
  • 138. WAS  SCID  CVID  HIV  HTLV-1
  • 139. X-linked defect in the ability to mount an IgM response to capsular polysaccharides  (Aldrich = ↑ IgA)  normal IgE levels  low IgM levels.  Triad of symptoms includes: (WIPE)  recurrent pyogenic Infections,  thrombocytopenic Purpura,  Eczema  IL-4
  • 140. Framshift/Nonsense mutation  Adenosine deaminase deficiency  T-cell>B-cell  Bacterial infections  Fungal infections
  • 141. Late onset  Frameshift/Missense mutation  Normal numbers of circulating B cells  Tyrosine Kinase deficiency
  • 142. T-cell>B-cell  CD4 rich  Brain  Testicles  Cervix  Blood vessels
  • 143.
  • 144. Amytal  Rotenone
  • 145. Malonate
  • 146. Antimycin D
  • 147. CN-  CO  Chloramphenicol
  • 148. Oligomycin
  • 149. DNP  Free Fatty acids  Aspirin
  • 150. Physical uncoupler
  • 151. Plasma  Urea cycle  Collecting ducts  Glutaminase
  • 152.  Azithromycin 1 gram po  Ceftriazone 250 mg im
  • 153. Azithromycin 1 gram po
  • 154. Ketoconazole 150mg
  • 155. Difluccan 1 pill
  • 156. Metronidazole 2 grams
  • 157. Metronidazole 2 grams
  • 158.  Ceftriaxone 250 mg im  Cefixime 400 mg po  Cefoxitin 400 mg po
  • 159.  Ciprofloxacin 500 mg po  Ofloxacin 400 mg po  Gatifloxacin 400 mg im
  • 160. Phosphorylase (Pi)  Debranching enzyme  Alpha-1,6 –Glucosidase  Phosphatase
  • 161. Glycogen synthase  Branching enzyme
  • 162. Glycogen alpha-1,4 glycosyl transferase  Glycogen alpha-1,6 glycosyl transferase
  • 163. Phosphorylase (Pi)
  • 164. pO2?  Normal  pCO2?  Normal or increased  pH?  Decreased
  • 165. pO2?  Decreased  pCO2?  Decreased  pH?  Increased
  • 166. Respiratory acidosis
  • 167.  Fabry’s  α – galactosidase  Krabbe’s  Galactosylceramide  Gaucher’s  β – glucocerebrosidase  Niemann – Pick  Sphingomyelinase  Tay-Sachs  Hexosaminidase  Metachromatic leukodystrophy  Arylsulfatase  Hurler’s  α – L – iduronidase  Hunter’s  Iduronidase sulfatase
  • 168. PAIR  Psoriasis  Ankylosing spondylitis  IBD (Ulcerative colitis)  Reiter’s Syndrome
  • 169. HLA-13
  • 170. Von Gierke’s  Glucose – 6 – phosphate  Pompe’s  α – 1 – 4 glucosidase  Cori’s  Debranching enzyme  McArdle’s  Glycogen phosphorylase
  • 171. Pyruvate?  Glycine  Alanine  Serine  Acetyl CoA ?  Phenylalanine  Isoleucine  Threonine  Tryptophan  Lysine  Leucine
  • 172. Alpha-KG ?  Glutamate  Glutamine  Succinyl CoA?  Phenylalanine  Tryptophan  Tyrosine
  • 173. Fumerate ?  Proline  Oxaloacetate?  Aspartate  Asparigine
  • 174. Oxidation – 7 NADH – 21 ATP  Hydration  Oxidation - 7FADH – 14 ATP  Thiolysis – 8 AcCoA – 96ATP 131 ATP – 2 (to bring it in)
  • 175. pO2? Decreased  pCO2? Decreased  PCWP? Decreased (b/c it’s a pressure problem)  Respiratory Rate? Increased  pH? Increased  SZ? Increased
  • 176. ACTH  ADH  PTH  TSH  ANP
  • 177. Anti-smith  Anti cardiolipin  Anti-ds DNA  SLE
  • 178. Anti – histone?  Drug induced SLE
  • 179. Anti-topoisomerase?  PSS (Progressive Systemic Sclerosis)
  • 180. Anti TSH receptors?  Graves
  • 181. Anti-centromere?  CREST
  • 182. Anti-GBM?  Goodpasture’s
  • 183. Type IV collagen
  • 184. Anti-mitochondria?  Primary biliary cirrhosis
  • 185. Anti-hair follicle?  Alopecia areata
  • 186. Anti-IgG?  Rheumatoid arthritis
  • 187. Anti-myelin receptors?  MS
  • 188. Anti-gliaden?  Anti-gluten?  Celiac sprue
  • 189. Anti-islet cell receptor?  DM Type I
  • 190. Anti-melanocyte?  Viteligo
  • 191. Anti-ACh receptor?  MG
  • 192. Anti-ribonuclear protein?  Mixed Connective Tissue dz (MCTD)
  • 193. Anti-parietal cell receptor?  Pernicious anemia
  • 194. Intrinsic factor
  • 195. Anti-epidermal anchoring protein receptors?  Pemphigus vulgaris
  • 196. Intercelluar junctions of epidermal cells
  • 197. Anti-epidermal basement membrane protein?  Bullous pemphigoid
  • 198.  IgG sub-epidermal blisters  Oral blisters
  • 199. Anti-platelet?  ITP
  • 200. Glycoprotein IIb/IIIa
  • 201. Anti-thyroglobulin?  Anti-microsomal?  Hashimoto’s
  • 202. Anti-smooth muscle?  Anti-scl-70?  Scleroderma
  • 203. Anti-rho (SS-A)?  Anti-la?  Sjogren’s
  • 204. Anti-proteinase?  C-ANCA?  Wegener’s
  • 205. P-ANCA?  Polyarteritis nodosa
  • 206.  Hepatitis B antigen  IgM
  • 207.  Papilloma virus? Cervical CA  EBV? Burkitts Nasopharyngeal CA  HepB & C? Liver CA  HIV? Kaposi’s Sarcoma
  • 208. Clot in front of renal artery?  Renal artery stenosis  Clot off whole renal artery?  Renal failure  Inflamed glomeruli?  Glumerulo nephritis  Clot in papilla?  Papillary necrosis  Clot off medulla?  Interstitial nephritis  Clot off pieces of nephron?  Focal segmental GN (HIV, drug use association)  Clot off lots of nephrons?  Rapidly Progressive GN
  • 209. Min. change disease  2 wks post URI
  • 210. Goodpasture’s
  • 211. Wilm’s tumor
  • 212. Adenocarcinoma
  • 213. Cyst
  • 214. Focal Segmental GN
  • 215. Membranous GN
  • 216. What does tPA, Streptokinase, Urokinase inhibit?  Aminocaproic acid  What doe Warfarin inhibit?  Vitamin K  What does Heparin inhibit?  Protamine Sulfate
  • 217. IV push?  20mg  Drip?  40mg
  • 218. IV push?  750K  Drip?  750K
  • 219. Used ONLY for such things as: ▪ Feeding tubes ▪ Central lines ▪ Fistulas
  • 220. Loss of a patch of hair
  • 221. Loss of ALL hair on head “bald”
  • 222. Loss of hair on entire body “hairless”
  • 223. Pneumonitis with endocarditis = pulmonary infiltrate with severe eosinophilia
  • 224. PIE syndrome
  • 225.  Necator americanus  Ankylostoma duodenale  Shistosomiasis  Strongyloides  Ascaris lumbricoides
  • 227. Homocystine methyl transferase  Methyl malonyl-coA mutase
  • 228. No male transmission  All females pass it on
  • 229.  Burn patients  Cystic fibrosis  DM  Neutropenic patients
  • 230. cover 1x for Staph aureus during 1st week  cover 2x for Pseudo after 2nd week
  • 231. Increased pO2  Delayed opening/closing of the pulmonary value  Increased volume in the right ventricle
  • 232. Blood transfusion  Increased Tidal Volume  Giving O2  Right sided heart failure  Pregnancy due to increase volume  IV fluids  ASD/VSD  Deep breathing  Hypernateremia  SIADH  Pulmonary regurge  Pulmonary stenosis  Right bundle branch block
  • 233. PIMP TRAP  Pericardium  Intracranial  Mediastinum  Pleural cavity  Thighs  Retroperitoneum  Abdominal cavity  Pelvis
  • 234. Gram +  Basement membrane suppressor  Works on simple anaerobes  The #1 cause of anaphylaxis  Causes interstial nepritits  Causes nonspecific rashes  Acts as a hapten causing hemolytic anemia
  • 235. Penicillin
  • 236. GIFTS  Granuloma  Ileum  Fistula  Transmural  Skip Lesion
  • 237.  Prodromal period before symptoms = 1-3 weeks  Why is there a prodromal period?  Because must switch to positive stranded before replication
  • 238. Symptoms within 1 week or less  EXCEPTIONS:  Hanta  Ebola  Yellow fever  They are -ve stranded = don’t have to switch to positive before replicating
  • 239. Transposition of the great arteries  Tetrology of Fallot  Truncus Arteriosus  Tricuspid Atresia  Total anomalous pulmunary Venous Return  Hypoplastic Left heart syndrome  Ebstein’s anomaly  Aortic atresia  Pulmonary atresia
  • 240. Tetrology of Fallot
  • 241. Ebstein’s Anomaly
  • 242. Hypokalemia  Hypermagnesemia  Hypercalcemia (except atrium)  Hypernatremia
  • 243. Hyperkalemia  Hypomagnasemia  Hypocalcemia (except atrium)  Hyponatremia
  • 244. TLCFN (Tender Loving Care For Nancy)  TPP – Thiamin – B1  Lipoic Acid – B4  CoA – Pantothenic acid – B5  FAD – Riboflavin – B2  NAD – Niacin – B3
  • 245. Bruton’s Agammaglobulinemia  CGD (NADPH def)  DMD  G6PD  Hemophilia  Lesch-Nyhan  Vit D resist. Rickets (X-linked dominant)  Fabrys  Hunters
  • 246. Bruton’s agammaglobulinemia  CVID (Common Variant Imm. Def)  Leukemias  Lymphomas  SCID  WAS  Job Buckley Syndrome
  • 247. Bruton’s agammaglobulinemia
  • 248. SCID  WAS  Job Buckley Syndrome
  • 249. Scabies  Lichen Planus  Urticaria  Dermatitis Herpetiformis
  • 250. L-myc?  Small cell lung Ca  C-myc?  Promyelocytic leukemia (Burkitt’s lymphoma)  N-myc?  Neuroblastoma  Small cell lung CA  C-able?  CML  ALL
  • 251. C-myb?  Colon CA  AML  C-sis ?  Osteosarcoma  Glioma  Fibrosarcoma
  • 252. C-erb B2?  Epidermal growth factor receptors  CSF-1 ?  Breast
  • 253. Erb-B2?  Breast CA  Ovarian CA  Gastric CA  Ret?  Medullary CA of thyroid  Men II & III  Papillary carcinoma
  • 254. Ki-ras?  Lung CA  Colon CA  Bcl-2?  Burkitts  Follicular lymphoma  Erb?  Retinoblastoma
  • 255. Relax hCG Is HOPE  Relaxin  hCG  Inhibin  Human placental lactogen (HPL)  Oxytocin (drug lactation, pit gland prod it also)  Progesterone  Estrogen
  • 256. Severity of microscopic change  Degree of differentiation
  • 257. Degree of dissemination of tumor  What the surgeon sees
  • 258. Urticaria/Hives?  Any CA, especially lymphoma  Pagets Ds (ulcers around nipples)  Seborrheic keratosis (waxy warts)?  Colon CA  HIV if sudden increase in number  Normal with aging
  • 259. Actinic keratosis?  Dry scaly plaques on sun-exposed skin  Squamous Cell CA of skin  Dermatomyositis?  violacious, heliotropic rash, malar area  Colon CA
  • 260. Akanthosis nigricans?  dark lines in skin folds  Any visceral CA  End organ damage  Erythema nodosum?  ant aspect of legs, tender nodules  Anything granulomatous  NOT assoc. w/ bacteria
  • 261. Apo E  Apo A  Apo CII  L-CAT  lecithin cholesterol acetyl transferase  Cholesterol  from periphery to liver
  • 262. Apo B-100  Apo E  Apo C II  Triglcyerides (95%)  Cholesterol (5%)
  • 263. Apo B-100  Apo E  Apo CII  Triglycerides (< VLDL)  Cholesterol (>VLDL)
  • 264. Apo B-100  Cholesterol  from liver to tissue  NOT a good thing!!!!!
  • 265. Apo A  Apo B-48  Apo E  Apo C II  Triglycerides from:  GI to liver (25% of the time)  GI to endothelium (75% of the time)
  • 267. Clue = HEAL  Heart?  Machinery murmur  Elbow?  Fistula from dialysis in renal disease  Abdomen/Brain?  Von Hippel-Lindau = clot off with coils  Increase incidence of Renal cell CA on chrom 3  Lungs?  Osler Weber Rendu Syndrome
  • 268. Glucose > 200  Age > 55  LDH >350  AST > 250  WBC > 16,000
  • 269. Calcium <8 mg/dl  HCT drop > 10%  O2 < 60 (PaO2)  Base deficit > 4  BUN > 5 mg/dl  Sequestration > 6L
  • 270. CF  Glaucoma  Painful, red, teary eye
  • 271. Problem with sense of taste
  • 272. Metronidazole  Clarithromycin  Zinc deficiency
  • 273. Flushing  Wheezing  diarrhea
  • 274. Serotonin  5-HIAA
  • 275. Pancreas  Ileum
  • 276. Mnemonic: BEDS  Botulinum  Erythrogenic toxin  from strep pyogenes  Diptheria  Salmonella/shiga like toxin  Has O antigen
  • 277. I sprayed ORTHO on my BUNYA at the ARENA down in REO to kill SEGMENTED WORMS
  • 278. ICAMs  Integrins  Selectins
  • 279. Bind proteins
  • 280. Stop the leukocytes
  • 281. Bind carbohydrates  Mediate the rolling to slow leukocytes down
  • 282. Homing of lymphocytes  tells lymphocytes where to go  Inflammation  Cell-cell interaction
  • 283. Contact
  • 284. Neutrophils  The next cells to show up are?  B-cells  What do B-cells make?  IgM
  • 285. M Σ  Three  IgM peaks at what day?  14  When does IgM leave?  In 2 months
  • 286. IgG  When does IgG peak?  In 2 months  When does IgG leave?  In 1 year
  • 287. MEMORY
  • 288. IgG with 5x concentration  Has the highest affinity  When does IgG peak?  In 5 years  When does IgG leave?  In 10 years
  • 289. IgG
  • 290. IgG
  • 291. IgG
  • 292. IgE  Uh huh! You thought all of them were IgG…
  • 293. Smoking  Alcohol  Nitrites  Japanese
  • 294. Smoking  Aniline dyes  Benzene  Aflatoxin  Cyclophosphamide  Schistosomiasis  2 diseases:  Von Hippel-Lindau  Tubular sclerosis
  • 295. Nitro Blue Tetrazolium test  What is it used for?  Screening CGD  What does a –ve test indicate?  +ve for the disease
  • 296. Howell-Jolly?  Sickle cell  Heinz?  G-6-P-D  Zebra?  Niemann pick
  • 297. Donovan?  Leishmaniasis  Mallory?  Alcoholism  Negri?  Rabies
  • 298. Councilman?  Yellow fever  Call-exner?  Ovarian tumors ▪ granulosa origin
  • 299. Lewy?  Parkinsons  Pick?  Pick’s disease  Barr body?  Normal female
  • 300. Aschoff?  Rheumatic fever  Cowdry type A inclusions?  Herpes virus  Auer rods?  AML
  • 301. Globoid?  Krabbe’s lysosomal storage disease  Russell?  Multiple myeloma
  • 302. Schiller-Duvall?  Yolk sac tumor  Basal bodies?  Only found in smooth mm
  • 303. Mnemonic? ACID  Type I  Anaphylaxis/Atopic  Type II  Cytotoxic (Humoral)  Type III  Immune complex mediation  Type IV  Delayed hypersensitivity/Cell mediated
  • 304. Atopic  IgE (Asthma) binds to mast cell  IgA activates IP3 cascade degrading mast cells
  • 305. Humoral  What are examples of type II?  Rh disease  Goodpastures  Autoimmune hemolytic Anemia  All Autoimmune diseases  except RA and SLE
  • 306. Ag-Ab complement  What are examples of Type III?  RA  SLE  Vasculitides  Some GN?
  • 307. Cell mediated  What are examples of Type IV?  TB skin test  Contact dermatitis  Transplant rejection
  • 308. Appendix  Epithalamus  Palmaris longus  muscle  Pancreatic polypeptide  hormones in F-cells
  • 309. Goodpastures  Wegeners  DM  HTN
  • 310. Vasculitis  AIDS
  • 311. Tx?  N-acetylcysteine  Test used to detect CF?  Pilocarpine sweat test  What ion does this test measure?  Cl-  Definitive presence of disease has a test value of what?  >60
  • 312. What is the value in a normal person?  <20  What is the value in a heterozygous person?  30 – 60  What chromosome is the CF gene on?  Chrom 7  What Second messenger is used?  IP3/DAG
  • 313. Bacillus anthracis  Clostridium perfringens  Clostridium tetani  Clostridium melangosepticus  What is the chemical in spores?  Calcium dipocholinate
  • 314. Lactic acid
  • 315. Alpha-receptors
  • 316. Cold agglutinin testing  IgM
  • 317. AA amyloid?  Chronic active disease  AL amyloid from Ig light chain?  Myeloma
  • 318. Beta 2 microglobulin?  Chronic hemodialysis  AA amyloid from SAA?  Nephrotic hereditary forms ▪ eg. Mediterranean fever
  • 319. Pre-albumin/transthyretin?  Cardiomyopathic hereditary forms ▪ senile systemic amyloidosis  Neuropathic hereditary syndromes
  • 320. ANP fibrils are caused by?  Senile cardiac amyloisosis  Cerebral amyloid in Alzheimer’s disease/Down’s?  Cerebral amyloidosis
  • 321. Calcitonin precursors?  Medullary CA of thyroid  AL from light chains?  Isolated, massive, nodular deposits ▪ lung, skin, urogenital tract
  • 322. Frontotemporal dementia
  • 323. Atrophy of frontal and temporal cortex with sparing of remaining neocortical regions
  • 324. Altered neurofilaments  Tau protein  ubiquitin
  • 325. Prevents pre-synaptic release of Ach  How do babies get it?  From spores in honey or molasses  How do adults get it?  From canned food
  • 326. Lethal factor – (black necrosis)  Protective factor  Edema factor
  • 327. Anthracis  Cereus
  • 328. B1-selective?  A–M  Non-selective?  N–Z  Exceptions?  Carbetalol and Labetolol are non-selective
  • 329. Problem in proximal tubule  Can’t reabsorb  Low energy state causing anemia  Can be due to old tetracycline
  • 330. In the collecting duct of the kidney  What does glutmainase help the kidney absorb?  Ammonia if the liver fails
  • 331. Hilum  Pelvic brim  Entering the bladder
  • 332. SLE  Endometrial CA  Cervical CA
  • 333. Carbamoyl synthase I  Where is it found 90% of the time?  Liver  Where is it found 10% of the time?  Collecting duct of the kidney
  • 334. -ve charge
  • 335. +ve charge  What is it used for?  Reversing the effects of heparin
  • 336. T-cells and macrophages  Schistocytes  Decreased platelets  Decreased RBCs  Bleeding from mucosal surfaces  Bleeding from skin and GI  Petechiae  Ecchymoses
  • 337. The following deveop:  Clots  DIC  Pulmonary embolism  DVT  MI  Stroke
  • 338. Tachypnea and SOB  Most common cause of death?  Heart failure
  • 339. Inhibits the translocation step of ribosomal protein synthesis
  • 340. Inhibits ribosomal peptidyl transferase in prokaryotes
  • 341. Inhibits elongation by binding to “A” site and prematurely terminating chain growth in pro and eukaryotes
  • 342. Causes misreading of code during initiation in prokaryotes
  • 343. Prevents binding of aminoacyl-t-RNA to ribosome on prokaryotes therefore inhibiting initiation
  • 344. Inhibits ribosomal peptidyl transferase in eukaryotes  cell wall inhibitor
  • 345. Blocks B-subunit of RNA polymerase  Prophylaxis for contacts of N. meningitidis
  • 346. Cell wall inhibitor  Binds irreversibly to Phopholipase carrier  Bacteriacidal  Covers all gram +ves  Linezolid
  • 347. Blocks vitamin k dependent gamma- carboxylation of prothrombin and factors 2, 7, 9, 10, proteins C & S
  • 348. Blocks translation by binding the 50S subunit
  • 349. What type of hemolysis is alpha hemolysis?  Partial hemolysis  What color is it’s zone?  Green  What type of hemolysis is beta-hemolysis?  Complete hemolysis
  • 350. What color is it’s zone  Clear  eg. Streptokinase  What type of hemolysis is gamma-hemolysis?  No hemolysis  What color is it’s zone?  Red
  • 351. High urine PH (??????not sure about this)  Acidosis  UTI s  Stones  Babies die < 1 yr old
  • 352. Acidosis  urine PH = 2, normal is 5-6  Hypokalmia  Patients have NO carbonic anhydrase
  • 353. It is a combination of RTA I & III  Normal urine pH  Hypokalemia
  • 354. Seen in diabetics  Hyperkalemia  NO aldosterone b/c JG apparatus has infarcted
  • 355. Viridans  Mutans  Sanguis  Salivarius  Bovis
  • 356. Viridans
  • 357. Viridans
  • 358. Mutans
  • 359. HTN  Hematuria  RBC casts
  • 360. Increase Edema  Increase Lipidemia  Increase Cholesterolemia  Increase Coagulability  Decrease serum Albumin  Increase urinary Albumin
  • 361. Strep. Pneumo  What is the #2 cause?  Hemophilus influenza  What is the #3 cause?  Neisseria meningitides
  • 362. Viruses  Which are secondary to what?  Bacterial infections  What is the #2 method to paralyze cilia?  Smoking
  • 363. Staph aureus  Clostridium perfringens  Bacillus cereus….from what?  Fried rice
  • 364. Preformed
  • 365. Release of glycine from spinal cord  What physical finding would you see?  Lock jaw  What is the tx?  Antitoxin and Toxoid  Where is it injected?  Injected in different areas of body
  • 366. E. coli  Followed by?  Proteus  Followed by?  Klebsiella
  • 367. Staph saprophyticus  Why?  They stick things in themselves  18-24 yoa?  Staph saprophyticus  Why?  Because they stick things inside themselves  Why no UTI’s after 24?  Because women are use to penises and Staph saprophyticus lives on penis (becomes part of normal flora).
  • 368. Osteomyelitis  Because of what?  Collagenase
  • 369. Staph. aureus
  • 370. Shock  Rash  Hypotension
  • 371. E. coli  Then?  Proteus  Then?  Klebsiella
  • 372. Group B Strep (agalactiae)  E. coli  Listeria
  • 373. Group B Strep (Strep. Agalactiae)  E. coli  Listeria
  • 374. Clostridium melanogosepticus  Strep bovis  What color pigment is produced?  Black
  • 375. IgG  What about Avidity?  IgM
  • 376. Virus inject it’s DNA into bacteria
  • 377. Virus injects it’s DNA into it bacteria in a hospital or nursing home setting, then becomes deadly.
  • 378. Bacteria with Pili
  • 379. Citrobacter
  • 380. Hemophilus influenza  Neisseria
  • 381. C3
  • 382. Gram negative bacteria
  • 383. BUN  >20  Fractional Na+ excertion  <1%  Creatine  >40
  • 384. BUN  10-15  Fractional Na+ excretion  >2%  Creatinine  <20
  • 385. Pavementing  Margination  Diapediesis  Migration
  • 386. PFK-1
  • 387. fructose-1,6-bisphosphatase  NOT Pyruvate Carboxlyase
  • 388. Viral  If resistant to tx, what next?  Fungal  Mycobacterium  Protozoa  Parasite  Neoplasm
  • 389. Step. Group B  Strep agalactiae  Strep. Pneumonia  Herpes simplex virus  Neisseria gonorrhea  Chlyamydia
  • 390. Perivascular angiofibromata
  • 391. Primary Adrenocoritcal Insufficiency
  • 392. Ochronosis
  • 393. Allergic Granulomatosis  Angiitis
  • 394. Ameloblastoma  What is Ameloblast?  Tooth material
  • 395. Regional enteritis  Granulomatous ileitis  Ileocolitis
  • 396. Subacute Granulomatous Thyroiditis
  • 397. Comedo Ca
  • 398. Mucolipidosis II
  • 399. MLNS  Mucocutaneous Lymph Node Syndrome
  • 400. Interstitial cells
  • 401. Sustentacular cells
  • 402. Giant cell arteritis (granulomatous)
  • 403. Hyperviscosity syndrome
  • 404. Oral  Trigeminal ganglia
  • 405. Genital  Sacral plexus
  • 406. Varicella zoster
  • 407. EBV  Mononucleosis  Burkitt’s
  • 408. CMV  Inclusion bodies
  • 409. Roseola  Duke Disease  Exanthem subitum
  • 410. Pityriasis rosea
  • 411. Kaposi’s sarcoma
  • 412. What is the MOA?  Interferes with normal synthesis and gama carboxylation of Vit. K dependent clotting factors via vitamin K antagonism.  Is it long or short acting?  Long half-life  8-10 hours to act
  • 413. Clinical use?  Chronic anticoagulation  Contra-indication?  Pregnancy because it can cross the placenta
  • 414. What pathway does it affect?  Extrinsic pathway  What does it do to PT?  Prolongs  PT
  • 415. What are the toxicities?  Bleeding  Teratogenic  Drug-drug interactions  How is it activatied?  Tissue activated
  • 416. Administration?  po
  • 417. II  VII  IX  X  Protein C  Protein S
  • 418. What is the MOA?  Catalyzes the activation of antithrombin III  Decreases thrombin and Xa  Is it long or short acting?  Short half-life  Acts immediately
  • 419. Clinical use?  Immediate anticoagulation of pulmonary embolism, stroke, angina, MI, DVT.  Contra-indication?  Can be used during pregnancy because it does not cross the placenta
  • 420. What pathway does it affect?  Intrinsic pathway  What value should you follow?  PTT
  • 421. What are the toxicities?  Bleeding  Thrombocytopenia  Drug-drug interactions  How is it activatied?  Blood activated
  • 422. Administration?  I.V.  Drug of choice for what?  DVT
  • 423. What is good about the newer low-molecular- weight heparins?  They act more on Xa  Have better bioavailability  Have 2 to 4 times longer half life  Can be administered subcutaneously and without laboratory monitoring.
  • 424. Protamine sulfate
  • 425. Dimercaprol
  • 426. Flumazenil
  • 427. Pralidoxime
  • 428. Deferoxamine
  • 429. Naloxene
  • 430. Bicarbonate  Doxapram
  • 431. Activates the respiratory center in the brain
  • 432. Provostatin  Atrovastatin  Lovastatin  Simvastatin
  • 433. Provastatin
  • 434. Atrovastatin  Lovastatin  Simvastatin
  • 435. HMG-CoA reductase  When is it most active?  8:00pm on
  • 436. Cholestipol  Cholestyramine  If nothing works what do you give?  Probucol  Niacin
  • 437. Flushing  Itching
  • 438. Cholestipol  Cholestyramine
  • 439. 1.Pancreatitis  Due to What?  ETOH 2.Kidney stones  Due to What?  Alcohol
  • 440. 3.AAA  How is this described?  Ripping pain down back 4.Ischemic bowel  What is symptom?  Bloody diarrhea
  • 441. Small cell Ca of lung  Increased intracranial pressure  Pain (most common)  Drugs  Hypoxic Lung Disease/Restrictive Lung disease
  • 442. Carbamazepine
  • 443.  Melanocytes  Odontoblasts (predentin)  Tracheal Cartilage  EnteroCHROMOFIN Cells  Laryngeal/Tracheal cartilage  Parafollicular cells of thyroid - Pseudounipolar cells  All Ganglion cells (Schwann, Adrenal medulla)  Schwann Cell  Spiral membrane of heart
  • 444. 220 - age
  • 445. RTA  Diarrhea  Diabetic ketoacidosis (DKA)
  • 446. Parainfluenza  Adenovirus  Influenza  RSV
  • 447. Bronchiolitis
  • 448. Diarrhea  Dermatitis  Dementia  Death
  • 449. Cysteine  Ornithine  Lysine  Arginine
  • 450. Phase 0?  Depolarization  Phase 1?  No name  Phase 2?  Plateau phase (A-V node)
  • 451. Phase 3?  Repolarization  Phase 4?  Automaticity (S-A node)
  • 452. Wider QRS
  • 453. Wider P-wave  Longer PR interval
  • 454. Calcium oxalate (phosphate) stones  Struvite stones  Uric acid stones  Cysteine stones  Oxalate stones
  • 455. 80%
  • 456. 3 y/o white male?  CF  5 y/o black male?  Celiac Sprue
  • 457. Adult male?  Whipple’s  Adult male or female?  Crohn’s
  • 458. In 0-20 y/o?  Malabsorptin  What age do they die?  Young
  • 459. What type of crystals are present?  Calcium pyrophosphate  Where are they found?  Joint spaces
  • 460. Who gets it?  Older patients M=F  Tx?  Colchicine
  • 461. VSD  ASD  PDA  Coarctation
  • 462. VSD  Mitral
  • 463. ASD
  • 464. PDA
  • 465. Coarctation
  • 466. Coarctation
  • 467. Pyruvate carboxylase  PEP carboxykinase  F-1,6 dPhosphatase  G-6-Phosphatase
  • 468. Hexokinase  PFK-1  Pyruvate kinase
  • 469. Prolactin  GH
  • 470. Nocardia
  • 471. Cryptosporidium
  • 472. Mycotic aneurysm  Roth spots  Janeway lesions  Osler’s nodes  Splinter hemorrhages  Endocarditis
  • 473. Janeway lesions?  Toes  Osler’s nodes?  Fingers  Roth spots?  Retina
  • 474. Strep. viridans
  • 475. Acetaminophen  Reye Syndrome  Pregnancy
  • 476. Alcohol
  • 477. Staph. Aureus  Pseudomonas
  • 478. Pseudomonas  Diptheria
  • 479. It ADP ribosylates EF2 inhibiting protein synthesis  Is it Gram +/-?  +  Where and how does it get its exotoxin?  From virus via transduction
  • 480. What does it cause?  Heart block  What do you give for Tx?  Antitoxin  Never scrape membrane
  • 481. Bullous?  Staph aureus  Pseudomonas  Centroacinar?  Smoking
  • 482. Distalacinar?  Aging  Panacinar?  Alpha-1 antitrypsin def
  • 483. 4 mo gestation?  Yolk sac  6 mo gestation?  Spleen, liver, flat bones
  • 484. 8 mo gestation?  Long bones  1 yr old?  Long bones
  • 485. Spleen can resume erythropoieses causing splenomegaly
  • 486. P-wave?  Ca+  QRS complex?  Na+  S-T?  Ca+
  • 487. T-wave?  K+  U-wave?  Na+
  • 488. QRS
  • 489. Widens P-wave  PR interval longer
  • 490. D W + A B A+B _ C D C+D A+C B+D ALL Sensitivity A/A+C Sensitivity: Truly Diseased People Always in the Specificity D/B+D Specificity: Truly Well People numerator PPV A/A+B + Predictive Value: Test +ve With DZ NPV D/C+D OR AD/BC - Predictive Value: Tested –ve w/o DZ A&D OR: Odds Ratio RR (A/All)/(C/All) RR: Relative Risk AR (A/All)-(C/All) AR: Attributed Risk
  • 491. Atrium contraction  Phase zero  Calcium
  • 492. AV Node  Phase 2  Sodium
  • 493. Septum  Phase 2  Sodium
  • 494. Anterior wall  Phase 2  Sodium
  • 495. Posterior wall  Phase 2  Sodium
  • 496. Ventricle  Phase 2  Calcium
  • 497. Ventricle  Phase 3  Potassium
  • 498. Ventricle  Phase 4  Sodium
  • 499. Narcolepsy  Allergy (hay fever)  Goodpasture  MS
  • 500. DM  Chronic active Hepititis  Sjogrens  SLE  Celiac sprue
  • 501. IDDM (DM Type 1)
  • 502. Rheumatoid Arthritis  Pemphigus Vulgaris
  • 503. JRA (JUV RA)  Pernicious anemia
  • 504. Nephrotic syndrome (Steroid induced)
  • 505. Celiac Disease
  • 506. Hemochromatosis  chromosome 6  point mutation Cystine to Tyrosine
  • 507. Myasthenia gravis
  • 508. Psoriasis
  • 509. Psoriasis  only if with arthritis  Ankylosing Spondylities  IBD  Ulcerative Cholitis  Reiter’s  Post gonococcal arthritis
  • 510. 21 alpha hydroxylase deficiency  Vit. D
  • 511. ADP ribosylates EF-2  Stops cell synthesis  Gr +ve  Gets exotoxin from virus via transduction  Heart block  Its toxoid therefore give antitoxin
  • 512. RSV (infants only)  Mycoplasma  Chlamydia pneumonia  Strep pneumonia
  • 513. Mycoplasma  Chlamydia pneumonia  Strep. Pneumonia
  • 514. Strep pneumonia  H. influenza  Anaerobes
  • 515. Strep pneumonia  Viruses  Anaerobes  H.influenza  Gr –ve rods
  • 516. Monomer in blood  Dimer in secretion  Located on mucosal surface  Found in secretion
  • 517. Only functions as surface marker for Mature B- Cell
  • 518. Immediate hypersensitivity/anaphylaxis  Parasite defense  Worms  Fc region binds to mast cells and basophils  Allergies  Does Not fix complement
  • 519. Highest affinity  Memory respond at day 3 five times the concentration  Peaks in 5 years last for 10 years  Opsonizes  Activates complement  2nd to show up in primary response  Only one to show up for secondary respond  Most abundant Ig in newborn  Antigenic differences in heavy chain and site of di- sulfide bond  4 subclasses G1 to G4
  • 520. Crosses placenta due to fc portion
  • 521. Most common sub-class deficiency  Patient susceptible to encapsulated organisms
  • 522. Most memory antibody
  • 523. Only IgG NOT fixing complement
  • 524.  Responds in primary response  Most efficient in agglutination and complement fixation  Defenses against bacteria and viruses
  • 525. MHC II
  • 526. IL-2  IF- Gamma
  • 527. IL-4  IL-5  IL-6  IL-10
  • 528. TH-1  TH-2
  • 529. CD8  CD8 becomes T-cytotoxic cells
  • 530. CD-3  For what?  Signal transduction  CD-2  For what?  Adherence
  • 531. T helper cells
  • 532. T cytotoxic cells
  • 533. Myeloperoxidase  NADPH  Will kill ALL Gr+ve  Ex..Hydrogen peroxide kills gr+
  • 534. Clue 4x7=28  CD-4  B-7  CD-28
  • 535. Increased Chylomicron  Deficiency of Lipoprotein lipase enzyme  Defect in liver only
  • 536.  Increased LDL  Two types IIa and IIb  Type IIa Receptor deficiency for LDL or missing B-100  Type II-b (LDL and VLDL problems) enzyme deficiency for LDL at adipose. Receptor problem for VLDL. Most common in General Population
  • 537. Increased IDL  Receptor problem for APO-E
  • 538. Increased VLDL  Lipoprotein lipase enzyme deficiency at adipose tissue
  • 539. Combination of Types 1&4  Increased Chylomicron and VLDL  Enzyme and receptor deficiency at C-II  Most common in diabetics
  • 540. Deposition of Cholesterol on elbows  Can cause what?  CAD
  • 541. Deposition of Triglycerides on eyelids, face  Can cause what?  Pancreatitis
  • 542.
  • 543. Little red spots w/ bright red margins  Sandpapery  RF- Jones critera
  • 544. Lymes disease  Target lesions (bulls eye)
  • 545. Morbiliform rash  Preceded by cough  conjunctiivitis
  • 546. Fever x 2 day  Followed by rash  ONLY ONE WITH RASH FOLLOWING FEVER (HHV 6)
  • 547. Anterior aspect of leg  Redness  Tender nodules
  • 548. Red macules, target lesions  Causes: allergy, viruses  Mild: MCC virus, #2 drugs (sulfas)  Moderate: Stevens-Johnsons Syndrome  Severe: Toxic epidermal necrolysis , skin peels off
  • 549. Scaly skin with oily shine on headline
  • 550. Stuck on warts  Due to aging
  • 551. HLA-B27  Extensor surfaces  Silvery white plaques  Scaly skin  Pitted nails
  • 552. STAGES  Red macules  Papules  Vesicles  Pustules then scabs  Different stages may appear at same time
  • 553. Rash and blisters on ant. thighs  Assoc. with diarrhea  Assoc. with flare up of celiac sprue
  • 554. SEEN WITH SALMONEALLA INFXN  Rose spots assoc. with intestinal fire
  • 555. Heliotropic rash
  • 556. Reddened area on skin w/ raised borders  DOES NOT BLANCH
  • 557. Redness  Itchy groin
  • 558.  Herald patch= dry skin patches that follow skin lines  HHV 7
  • 559. Hypopigmented macules on upper back  Presents in a V pattern  A.K.A. upside down christmas tree  Tx: Griseofulvin
  • 560. Linear excoriations on belt line and finger webs  What is the tx?  Lindane  Permethrin
  • 561. DiGeorges  What ion imbalance will they have?  Hypokalemia  What did not form?  3rd and 4th pharyngeal pouch  What chromosome?  Deletion on chromosome 22
  • 562. HIV  Also B-cell but less so
  • 563. NOT A FUNGUS  Non-Hodgkins form of cutaneous T-cell lymphoma
  • 564. Transport TG’s from GI to liver and endothelium
  • 565. Transports TG’s from liver to adipose
  • 566. Transports TG’s from adipose to tissue
  • 567. ONLY ONE THAT CARRIES CHOLESTEROL
  • 568. XANTHELASMA  Where are they located?  On eyelids and eyebrows
  • 569. Xanthomas  Where are they located?  elbows
  • 570. ONLY ONE MADE IN THE LIVER
  • 571. ARE BREAK DOWN PRODUCTS OF VLDL
  • 572. Gram -/+?  Pleomorphic gram (-) rods  What pattern?  “school of fish pattern”  What type is most common?  Type A  80%
  • 573. Capsule or no capsule?  non-encapsulated  Invasive or non invasive?  non-invasive
  • 574. Most common cause of what?  Sinusitis  Otitis  Bronchitis
  • 575. What is the 2nd most common type?  TYPE B  20%  Encapsulated or non encapsulated?  Encapsulated  What does it have in its capsule?  Polyribosyl phosphate in capsule  Contains IgA protease
  • 576. Invasive or non invasive?  Invasive  What does it cause most often?  #1 cause of epiglottitis  What are the signs of epiglottitis?  Stridor  Fever  Thumb sign on xray
  • 577. 0-2 months?  #1. Group B strep (agalactiae)  #2. E. coli  #3. Listera
  • 578. 2 Months- 10 years?  #1. strep pneumonia  #2. n. meningitides  (adolescent years only)
  • 579. 10yrs- 21 yrs?  #1. n. meningitides
  • 580. > 21 years old?  #1 S. pneumoniae
  • 581. At what age is it given?  Given at 2,4,6 months  What strain does it cover?  Covers 23 strains (98% cases)
  • 582. Indications?  Anyone> 65y/o  Anyone splenectomized  Sickle cell anemia  Anyone with end-organ damage  CF  RF  Nephrotic Syndrome
  • 583. MCC of all throat infections  #2 MCC of all what?  Skin infections except lines
  • 584. St. aureus?  Gold pigment  St. epidermidis?  White pigment  St. saprophyticus?  No pigment
  • 585. Strep. Pneumonia  pneumococcus
  • 586. Skin Infections?  Say Staph. Aureus  Throat Infections?  Say Strep. Pyogenes  Small Intestine Infections?  Say E. coli
  • 587. Job Syndrome:  IL-4  Hyper IgE  What do they look like?  Red hair  Fair complexion  Female
  • 588. NADPH-OXIDASE DEF (CGD)  NEUTROPENIA  MYLOPEROXIDASE  Job-Buckley Syndrome
  • 589. HbC antigen  HbS antigen
  • 590. HbC antigen  HbS antigen  HbC antibody
  • 591. HbS antigen ONLY
  • 592. HbS antibody ONLY
  • 593. HbC antibody  HbS antibody  HbS antigen
  • 594. IgG
  • 595. HbS antigen for >6months  Can be with or without HbS antibody
  • 596. HbE antigen
  • 597. HbE antibody
  • 598. NEGATIVE HbS antigen
  • 599. POSITIVE HbS antigen
  • 600. HbE antibody  IgM HbC antibody  What disappears?  HbS antigen
  • 601. 4 to 26 wks  Average @ 8wks
  • 602. 4 to 12 wks
  • 603. 4 to 20 wks
  • 604. YEARS
  • 605. MC infection?  CMV  MCC of death?  PCP  What is p41 used for?  Just a marker
  • 606. What does Gp120 do?  Attachment to CD4  What is Pol used for?  Integration  What is reverse transcriptase used for?  Transcription  What are p17 & p24 antigens used for?  Assembly
  • 607.  What is the normal CD4 count?  800-1200  What can the CD4 count be up to in children?  1500  When do you begin treating with 2 nucleotide inhibitors and 1 protease inhibitor?  <500  (child at 750)
  • 608. AIDS is defined as a CD4 count of what?  <200  With a CD4 count of <200 what do you tx for?  PCP  What do you treat for when CD count is <100?  Mycobacterium aviam intracellular
  • 609. Vitamin E  #1  Vitamin A  Vitamin C  Betakertine
  • 610. Parathyroid  Along with what other cofactor?  Mg+
  • 611. Hyperparathyroid  Increase Ca+  Decrease Phosphate  What will be the symptoms?  Goans  Moans  Bones  Stones
  • 612. Pseudotumor Cerebri  Increase CSF production from Chorichoid Plexus
  • 613. Pseucotumor cerebri
  • 614. Nightvision problems/nightblindness  Hypoparathyroidism  Decrease Ca+  Increase Phosphate
  • 615. THIAMINE  What do you get with a decrease in thiamine?  Beri Beri  What is the most common cause in US?  ETOH
  • 616. Wet Berry Berry  With heart failure  Dry Berry Berry  Without heart failure
  • 617. Wernicke’s Encephalopathy  Wernicke’s Korsakoff
  • 618. Alcoholic thymine deficiency of the Temporal Lobe
  • 619.
  • 620. 3 Dehydrogenases  Pyruvate dehydrogenase  Alpha ketoglutarate dehydrogenase  Branch chain amino acid dehydrogenase  Transketolase
  • 621. Riboflavin  What is a physical sign of this deficiency?  Angular stomatitis  Angular cheliosis  Corneal Neurovasculazations
  • 622. Milk  Also from FAD
  • 623. Niacin  What is the clue?  Diarrhea  Dermatitis  Dementia  Death
  • 624. Hartnup Disease  What is deficient in this disease?  Tyrptophan  What is typtophan needed for?  Needed for niacin formation
  • 625. Lipoic acid  What is the deficiency caused by this vitamin?  Not one
  • 626. Pantothenic acid  What is the deficiency caused by this vitamin?  You guessed it…nothing
  • 627. Pyridoxine  What is the deficiency caused by this vitamin?  Neuropathy  Seizures  Who do you need to give B6 to?  Patient on INH
  • 628. Sideroblastic
  • 629. ALL transaminases
  • 630. Cyanocobalamine  What is the deficiency caused by this vitamin?  Pernicious anemia  Neuropathy
  • 631. Pernicious anemia
  • 632. Methylmalonyl CoA Mutase  Homocysteine Methyl Transferase
  • 633. Neuropathy  Why?  Because it recycles myelin
  • 634. Megaloblastic anemia  What else is this enzyme needed for?  Nucleotide synthesis
  • 635. VITAMIN B2- RIBOFLAVIN deficiency
  • 636. DIARRHEA  DERMATITIS  DEMENTIA  DEATH
  • 637. PYRIDOXINE B6
  • 638. B12 CYANOCOBALAMINE
  • 639. Folate
  • 640. Megaloblastic anemia  With neuropathy?  NO NEUROPHATHY  What else is Folate used for?  Nucleotide synthase (THF)
  • 641. Ascorbate acid
  • 642. Collagen synthesis
  • 643. Scurvy
  • 644. Bleeding gums  Bleeding hair follicles
  • 645. Diet deficient in citrus fruit  Diet deficient in green vegetables  Over cooked green vegetables
  • 646. Controls Ca+  Absorbes Ca+ from GI  Reabsorbs Ca+ in Kidneys  Controls osteoblastic activity
  • 647. Ricketts  What does it cause in ADULTS?  Osteomalcia
  • 648. Lateral Bowing of the Legs  X-linked dominant
  • 649. Hair  Skin  Eyes  Protection against free radicals  #1 antioxidant
  • 650. Retinopathy
  • 651. Folate  Vitamin K  90%  Biotin  Panothenic acid  Helps with absorption of B12
  • 652. 1972  Protein C  Protein S  Which one has the shortest half-life?  Protein C  Which one has the 2nd shortest half-life?  7
  • 653. Chromium  Selenium  Manganese Molebdenum  Tin
  • 654. Insulin action
  • 655. Heart
  • 656. Manganese Molebdenum
  • 657. Hair
  • 658. Dysguzia  Decrease sperm  Dry hair  Dry skin
  • 659. Mg+
  • 660. Biotin
  • 661. Pyridoxine  B6
  • 662. ALL carboxylases
  • 663. ALL kinases  Parathyroid along with Vitamin A
  • 664. Muscle contraction  Axonal transport  2nd messengers
  • 665. Dorsal Columns  Cortical Spinal Tracts  Why are these affected?  Because they are the longest  Because they need the most myelin
  • 666. Maganese Molebdenum
  • 667. By the liver  Always Hepatotoxic
  • 668. By the kidney  Always nephrotoxic
  • 669. Pain  Pallor  Paresthesia  Pulselessness  Poikilothermia
  • 670. Lympangitis  Impetigo (not bullous)  Necrotizing fascitis  Erysepelas  Scarlet fever
  • 671. Lympangitis  Impetigo (not bullous)  Necrotizing fascitis  Erysepelas  Scarlet fever
  • 672. Staph epidermitis
  • 673. Staph aureus
  • 674. Absorption of Vit. B12  Synthesis of:  -Vitamin K  -Biotin  -Folate  -Pantothenic acid ▪ B5
  • 675. Trypsin cuts where?  cuts to R of  Arg  Lys  Chymotrypsin cuts where?  cuts to R of bulky aa’s (aromatics)  Phe  Tyr  Trp
  • 676. Elastase cuts where?  Cuts to R of (“SAG”)  Ser  Ala  Gly  CNBr cuts where?  Cuts to R of  Methionine
  • 677. Aminopeptidase cuts where?  Cuts to R of  amino acid terminal  Caboxypeptidase cuts where?  Cuts to L of  carboxy terminal
  • 678. MMR
  • 679. MMR & INFLUENZA
  • 680. Hepatitis B
  • 681. Hib  Diphtheria  Pertussis
  • 682. Strain 12
  • 683. Myeloperoxidase  NADPH Oxidase
  • 684. NADPH Oxidase  Which means they only kill what?  Kills only G -ve
  • 685. IL-1  IL-6??
  • 686. DDI>DDC  Pancreatitis
  • 687. Leigh’s Disease  What is another name?  Subacute necrotizing encephalomyelopathy  What are the signs & symptoms?  Progressively decreasing IQ  Seizure  Ataxia  What is the deficiency?  Cytochrome oxidase deficiency
  • 688. Leber’s Hereditary Optic Atrophy (LHON)  They all die
  • 689.  Listeria  What part is toxic?  Lipid A  Does it cross the placenta?  Yes
  • 690. T-cells & Macrophages, therefore, have granulomas
  • 691. Raw cabbage  Spoiled milk  Migrant workers
  • 692. Birth – 2 months  4 – 7 years old  Puberty
  • 693. DiGeorge’s Syndrome
  • 694. Lysine  Arginine
  • 695. Glutamate  Aspartate
  • 696. Phenylalanine  Isoleucine  Trptophan  Threonine
  • 697. Phenylalanin  Tyrosine  Tryptophan
  • 698. Met  Cyst
  • 699. Proline
  • 700. Gly
  • 701. Serine  Threonine  Tyrosine
  • 702. Asparagine  Glutamine
  • 703. Leu  Iso  Val
  • 704. Leu  Lys
  • 705. Psoriasis (with arthritis)  Ankylosing Spondylitis  Irritable Bowel Syndrome  Reiter’s Syndrome
  • 706. Psoriasis with out arthritis
  • 707. Strep. Pneumoniae  H. influenza  Neisseria catarrhalis
  • 708. Histaminase  Arylsulfatase  Heparin  Major Basic Protein
  • 709. In an Acute Reaction?  Histamine  In a Late Reaction ?  SRS-A  ECF-A
  • 710. 0 – 2 months?  chlamydia pneumonia
  • 711. Intersitital pneumonia
  • 712. High temperature with NORMAL pulse rate! (This should never be! Each degree ↑ in temp. → 10 beats/min ↑ in pulse rate)
  • 713.  FEVER  NONSPECIFIC ILLNESS  RECRUITS TH CELLS for LINKING with MHC II COMPLEX  SECRETED BY MACROPHAGES
  • 714.  MOST POTENT OF THE Interleukins  RECRUITS EVERYBODY  MOST POWERFUL CHEMO-ATTRACTANT  MUST BE INACTIVATED  When must you inactivate it?  PRIOR TO TRANSPLANTATION by cyclosporin  SECRETED BY TH1 CELLS
  • 715.  ENERGIZED MACROPHAGES  CAUSES B-CELL PROLIFERATION  LABELED BY THYMIDINE (USE POKEWEED MITOGEN OR ENDOTOXIN)  SECRETED BY ACTIVATED T CELLS
  • 716. B-CELL DIFFERENTIATION  RESPONSIBLE FOR CLASS SWITCHING  SECRETED BY TH2 CELLS
  • 717. They do exactly what IL-1 thru IL4
  • 718.  SUPPRESSES CELL-MEDIATED RESPONSE (tells macrophages and fibroblasts to stay away if bacterial)  INHIBITS MAC ACTIVATION
  • 719.  PROMOTES CELL-MEDIATED RESPONSE (recruits macs & fibroblasts if NOT bacterial)  ACTIVATES NK CELLS TO SECRETE IF-γ  INHIBITS IL-4 INDUCED IgE SECRETION  CHANGES TH CELLS to TH1 CELLS  secretes IL-2 & IF-γ → inhib. TH2, therefore, ↑ host defenses against delayed hypersensitivity
  • 720. Where is it from?  LEUKOCYTES  ↓VIRAL REPLICATION AND TUMOR GROWTH  ↑ NK ACTVITY  secretes perforins and granzymes to kill infected cell  ↑MHC CLASS I & II EXPRESSION  ↓ PROTEIN SYNTHESIS  translation inhibited, therefore, defective protein synthesis
  • 721. Increase NK activity  Increase MHC class I & II  Decrease protein synthesis  Decrease viral replication and growth
  • 722. Where is it from?  FIBROBLASTS  Increase NK activity  Increase MHC class I & II  Decrease protein synthesis  Decrease viral replication and growth
  • 723.  Where is it from?  T-CELLS & NK CELLS  ↑ NK ACTIVITY  ↑MHC CLASS I & II  ↑ MACROPHAGE ACTIVITY  CO-STIMULATES B-CELL GROWTH & DIFFERENTIATION  ↓ IgE SECRETION
  • 724. Where is it from?  MONOCYTES & MACROPHAGES  What is another name for TNF-alpha?  CACHECTIN  INDUCES IL-1  ↑ ADHESION MOLECULES & MHC CLASS I ON ENDOTHELIAL CELLS  PYROGEN  INDUCES IF-γ SECRETION  CYTOTOXIC/CYTOSTATIC EFFECT
  • 725. Where is it from?  T-CELLS  What is another name for it?  LYMPHOTOXIN  CYTOTOXIC FACTOR
  • 726. Where is it from?  SOLID TUMORS (CARCINOMA > SARCOMA)  MONOCYTES  What is another name for it?  TRANSFORMING GROWTH FACTORS
  • 727. What does it INDUCE?  ANGIOGENESIS  KERATINOCYTE PROLIFERATION  BONE RESORPTION  TUMOR GROWTH  What is it mainly for?  MAINLY FOR TUMOR GROWTH
  • 728. Where is it from?  PLATELETS  PLACENTA  KIDNEY  BONE  T & B CELLS
  • 729. What INDUCES it?  FIBROBLAST PROLIFERATION  COLLAGEN  FIBRONECTIN SYNTHESIS
  • 730. What INHIBITS it?  NK  LAK  CTL  T & B CELL PROLIFERATION
  • 731. What ENHANCES it?  WOUND HEALING  ANGIOGENESIS
  • 732. What does it suppress?  SUPPRESSES IR AFTER INFECTION & PROMOTES HEALING PROCESS  What is it mainly for?  MAINLY FOR WOUND HEALING
  • 733. LYMPHOKINE ACTIVATED KILLER CELLS
  • 734. CYTOTOXIC T-LYMPHOCYTES
  • 735. CNS  Heart  Skeletal muscle  Why does it affect these particular places?  Due to uneven cytokinesis during meiosis or oogenesis
  • 736. Who are affected?  All offspring  Who passes the disease?  MOM  Who has no transmission?  Dad
  • 737. Who does it show in?  Not parents  Siblings/uncles may show disease  When is onset?  Early in life (childhood diagnosis)  Is it complete on incomplete penetrance?  COMPLETE
  • 738. How are they acquired?  Almost ALL are inborn error of metabolism  When does it occur?  Only when both alleles at a locus are mutant
  • 739. How is it transmitted?  Horizontal Tm  Are there malformations present?  Physical malformations are uncommon  What type of defect?  Enzyme defect
  • 740. Who does it affect the most?  M=F  How does it manifest?  Heterozygote state  Who can transmit the disease?  Both parents
  • 741. Where is the new mutation?  Often in germ cells of older fathers  When is onset?  Often delayed (adult diagnosis)  Example = Huntington’s
  • 742. What is penetrance?  Reduced penetrance  How is it expressed?  Variable expressin  Different in each individual
  • 743. How is it transmitted?  Vertical TM  Is there malformation present?  Physical malformation common  What type of defect?  Structural
  • 744. Maternal grandfather  Maternal uncle
  • 745. What happens <24hrs?  Swelling  What happens at 24 hrs?  Neutrophils show up  What happens at day 3?  Neutrophils peak
  • 746. What happens at day 4?  T cells and Macrophages show up  What happens at day 7?  Fibroblasts show up  What happens in 1 month?  Fibroblast peak
  • 747. What happens at 3-6 months?  Fibroblasts are gone
  • 748. Lysosomal Inclusion Bodies
  • 749. Gauchers  Fabrys  Krabbe  Tay Sachs  Sandhoffs  Hurlers  Hunters  Neiman Pick  Metachromatic Leukodystropy
  • 750. Beta-Glucocerberosidase  What Accumulates?  Glucocebroside  Where?  Brain  Liver  Bone Marrow  Spleen
  • 751. Ask. Jew  Gargols  Gaucher cells  Macrophages looking like Crinkeled paper  Erlin myoflask legs  Pseudohypertrophy
  • 752. Alpha-galactosidase  What accumulates?  Ceramide Trihexoside
  • 753. X-Linked recessive  Presents with cataracts as a child  Presents with renal failure as a child
  • 754. Galactosylceramide B-Galactosidase  What accumulates?  Galactocerebrosidase  Where?  Brain
  • 755. Early death  Globoid bodies  Fat cells
  • 756. Hexoseaminidase A  What accumulates?  GM2 Ganglioside
  • 757. Ask. Jews  Cherry red macula  Death by 3
  • 758. Hexoseaminadase A & B
  • 759. Iduronidase
  • 760. Corneal Clouding  Mental Retardation
  • 761. Iduronate Sulfatase
  • 762. Mild mental retardation  No corneal clouding  Mild form of Hurlers  X-linked recessive
  • 763. Spingomyelinase  What accumulates?  Spingomyelin  Cholesterol
  • 764. Zebra bodies  Cherrry red macula  Die by 3
  • 765. Arylsulfatase A
  • 766. Visual Disturbance  Presents like MS in 5 to 10 years of age
  • 767. Von Gierkes  Andersons  Corys  McCardles  Pompes  Hers
  • 768. G-6-Pase Deficiency
  • 769. Big Liver  Big Kidney  Severe hypoglycemia  Can NEVER raise their blood sugar
  • 770. Branching enzyme deficiency
  • 771. Glycogen will be ALL LONG chains on liver biopsy
  • 772. Debranching enzyme
  • 773. Glycogen from liver biopsy will be ALL SHORT branches
  • 774. Muscle phosporalase
  • 775. Severe muscle cramps when exercising  High CPK
  • 776. Cardiac alpha-1,4 glucocydase
  • 777. Heart problems  Die early
  • 778. Liver phosphoralase
  • 779. Big Liver  NO big kidney
  • 780. Intraductal Ca
  • 781. AV Fistula  Vasodilation
  • 782. Tay Sachs  Sandhoffs  Niemann Pick
  • 783. CML
  • 784. Ewing’s sarcoma
  • 785. Burketts lymphoma
  • 786. Follicular lymphoma
  • 787. Sarcoid  Amyloid  Hemochromatosis  Cancer  Fibrosis  Thanks STAN!!
  • 788. Shistocytes  Burr cells  Helmet cells
  • 789. Splenomagely
  • 790. Adrenal  Liver
  • 791. G6PD
  • 792. Lead poisoning
  • 793. Iron deficiency  Anemia of Chronic disease  Lead poisoning  Hemoglobinopathy  Thallasemia’s  Sideroblastic anemia
  • 794. Genetic  AD
  • 795. Blood transfusions
  • 796. Hereditary Spherocytosis
  • 797. Acute hemorrhage  Anemia of Chronic Disease  Hypothyrodism  Early  Renal Failure
  • 798. Folate deficiency  B12 deficiency  Reticulocytosis  ETOH  Hemolytic Anemias  Chemo Treatment  Anticonvulsants  Myelodysplasia
  • 799. Phenytoin  Ethusuximide  Carbamyazapine  Valproate
  • 800. Sideroblastic anemia
  • 801. Something is wrong with the RBC membrane  Extravascular  Heridatary Ellitocytosis  Increased RET count
  • 802. Wilson’s Disease
  • 803. Hepato/Lenticular Degeneration  Kayser Fleishner Rings  Copper in eyes  Hepato = Liver  Lenticular = Movement problem
  • 804. Collagen synthesis
  • 805. Minky Kinky Hair Syndrome
  • 806. Epinephrine  Norepinephrine  Dopamine
  • 807. Tyrosine
  • 808. Adrenal Pheochromocytoma
  • 809. Blocks DNA gyrase (topoisomerase II)  Inhibits p450
  • 810. All Gram + including staph auerus  All Gram –  Atypicals
  • 811. Chlamydia  Ureoplasma  Mycoplasma  Legionella
  • 812. Cortisol  Epinephrine  Glucagon
  • 813. Glycosaminoglycan chain that helps form proteoglycans
  • 814. Glycosaminoglycan chain that helps form proteoglycans
  • 815. Inhibits dihydrofolate reductase  Inhibits DNA synthesis in the S phase of cycle.  Prevents reduction of folic acid needed to produce THF
  • 816. Purine nucleotide synthesis  Methylation of dUMP to for dTMP
  • 817. Obstructs one carbon methylation which deprives DNA polymerase of essential substrates
  • 818. CF  Galactosemia
  • 819. Defects in Glycolysis  Defects in Hexose Monophosphate Shunt
  • 820. B12
  • 821. B12
  • 822. Vitamin B6
  • 823. Vitamin C
  • 824. Occurs in the synthesis of Blood Clotting factors  Requires Vitamin K
  • 825. Thiamine
  • 826. Vitamin D
  • 827. Vitamin A
  • 828. Thiamine
  • 829. Olfactory  What is its function?  Sensory for smell  What if lesioned?  Anosmia  Where does it Exit/Enter the Cranium?  Cribriform plate  What does it innervate?  Nasal Cavity
  • 830. Optic  What is its function?  Sensory for sight  What if lesioned?  Anopsia  Visual field defect  Loss of light reflex with CN III  Only nerve affected by MS
  • 831. Where does it Exit/Enter the Cranium?  Optic Canal  What does it innervate?  Orbit
  • 832. Occulomotor  What are the functions?  Motor  Moves the eyeball in ALL directions  Adduction Most important action (MR)  Constricts the pupil (Spincter Pupillae)  Accomodates (Cililary Muscle)  Raises eyelid (Levator Palpebrae)
  • 833. What if lesioned?  Diplopia  Loss of parallel gaze  Dilated pupil  Loss of light reflex  Loss of near response  Ptosis
  • 834. Where does it Exit/Enter the Cranium?  Superior Orbital Fissure  What does it innervate?  Orbit
  • 835. Trochlear  What is its function?  Motor  Superior Oblique  Depresses and abducts the eyeballs  Intorts
  • 836. What if lesioned?  Weakness looking down w/ adducted eye  Trouble going down stairs  Head tilts away from lesioned side  Where does it Exit/Enter the Cranium?  Superior Orbital Fissure
  • 837. What does it innervate?  Orbit
  • 838. Trigeminal
  • 839. V1?  Opthalmic  V2?  Maxillary  V3?  Mandibular
  • 840. Mixed  General sensation (touch, pain, temperature) of the forehead, scalp, & cornea  What if lesioned?  Loss of general sensation of the forehead/scalp  Loss of blink reflex w/ VII  Where does it Exit/Enter the Cranium?  Superior orbital Fissure  Ophthalmic division
  • 841. What does it innervate?  Orbit  Scalp