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Pediatric neurology
Hari Shankar Meshram
Boring topic that too in afternoon
Waiting for the last slide
For passing marks
LP finding in APM and TBM
Apm : very low glucose, neutrophilic, very high
protein
Tbm : low glucose, lymphocytic, high protein,
cob web appearance
Neurofibromatosis has all of the following
except
1. Crowe sign
2. Lisch nodule
3. Brushfield iris
4. Neurofibroma
3
Recent
Tuberous sclerosis has all skin lesion except
1. Ash leaf macule
2. Adenoma sebacium
3. Shagreen patch
4. Angel kiss
4
Reversible gallbaldder sludge detected by
USG during treatment of bacterial
meningitis is caused by
1. Ceftriaxone
2. Cefotaxime
3. Vancomycin
4. Meropenem
1
Floppy baby
Spinal muscular dystrophy important genetic
cause of floppy baby invloves chromosome
1. 5
2. 6
3. 7
4. 9
1
AFP
Transverse myleitis involves mostly
1. Thoracic
2. Lumbar
3. Lumbosacral
4. Cervical
1 Afp causes are
polio, gullian barre
,transverse myelitis,
traumatic neuritis
floppy
Almond shaped eyes , with hyperphagia ,and
obesity and hypogonadism and history of
hypotonia in newborn period
1. Angelman
2. Prader willi
3. Gaucher
4. Tay Sach
2
Anterior fontonalle closes at months
1. 2 -3
2. 4-7
3. 9-12
4. 18-24
4
Total volume of CSF in neonate is
1. 50 ml
2. 100 ml
3. 25 ml
4. 150 ml
1 and 2 in
adult
Neural tube and neural migration
Which of the following is neuronal migration
defect
1. Shizencephaly
2. Myelomeningocele
3. SSPE
4. Gaucher
1
True about hydranencephaly
1.Absent cerebral hemisphere
2. Sun setting sign
3.Mental retardation
4.Normal sized ventricle
1
Hydranencephaly
CSF production rate per hour is
1. 20 ml
2. 10 ml
3. 25 ml
4. 15 ml
1
Normal ICP in a child is mmH20
1. 30 – 70
2. 50 – 80
3. 100 -150
4. 50 – 150
2 And 4 answer in case of adult
Choose one
1. 3.
2.
4. All of the above
Development
Razing at what age
1. 4 m
2. 6
3. 8
4. 10
1
Neck control at what age
1. 3
2. 6
3. 8
4. 10
1
Recently asked
9 cube tower at what age month
1. 40
2. 30
3. 20
4. 15
Answer is 2.
2 cubes 15 month
4 cubes 18 month
6 cubes 22 month
7 cubes 24
9 cube 30
10 cube 36 month
Casting at what age
1. 10 month
2. 6
3. 8
4. 12
4 casting means
throwing things
Mouthing and stranger anxiety and moros reflex
should disapper at what age
1. 4
2. 6
3. 8
4. 10
2
Object permenance, peek a boo game , waves bye
bye , and immature pincer grasp at what age
1. 4
2. 6
3. 9
4. 10
3
Separational anxiety, transitional object at what
age
1. 12
2. 18
3. 15
4. 10
2
13yr old child presented with fever and
altered sensorium with MRI shwoing
medial temporal lobe involvement
1. HSV
2. Neisseria
3. Cerebral malaria
4. Fungal meningitis
1
• Most common neurological sequele in
bacterial meningitis
1.Recurrent seizures
2 Hearing loss
3 Cognitive loss
4 Visual loss
2
Excessive irritability, crying,vomiting and
difficulty feeding with history of frequent
change in formula feeds suggests
1. Tay sach disease
2. Krabbes disease
3. Metachromatic leucodystrophy
4.Gaucher disease
2
A child with painful acroparastheisa and
angiokeratoma in skin with zebra bodies and
maltese cross in urine sample suggests
1. Tay sach disease
2. Krabbes disease
3. Fabry disease
4.Gaucher disease
3
Recent
• Seizures with aphasia as abnormal finding is
seen in
1. Absence seizures
2. West syndrome /Infantile spasm
3. Rolandic seizures
4. Landau klefner syndrome
4
Recent
• Hypsarrythmia is seen in
1. Absence seizures
2. West syndrome /Infantile spasm
3. Rolandic seizures
4. Landau klefner syndrome
2
Recent
• Periodic lateralised slowing in EEG is seen in
1. Absence seizures
2. Herpes simplex meningitis
3. Rolandic seizures
4. Landau klefner syndrome
2
Recent
• Multiple seizures of all types is seen in
1. Lennox gestaut syndrome
2. West syndrome /Infantile spasm
3. Rolandic seizures
4. Landau klefner syndrome
1
Choose one
1. 3.
2. 4. All of the above
Recent
• Lafora disease has
1. Absence seizures
2. Infantile spasm
3. myoclonic seizures
4. GTCS
3
Kernicterus in neonatal period is a major cause
of
1. Spastic diplegia CP
2. Spastic hemiplegia CP
3. Spastic quadriplegia CP
4. Athetoid CP
4
Most important risk factors for reurrence of
febrile seizures is
1. Age < 2 yrs
2. Family History
3. Seizures at peak of fever
4. Long prolonged fever before seizure
2
Passing mark q Cerebral palsy
Cerebral palsy in which upper limb is more affected
than lower limb is
1. Spastic diplegia CP
2. Spastic paraplegia CP
3. Spastic quadriplegia CP
4. Athetoid CP
1
Prematurity is a major cause of
1. Spastic diplegia CP
2. Spastic hemiplegia CP
3. Spastic quadriplegia CP
4. Athetoid CP
1
Birth asphyxia is a major cause of
1. Spastic diplegia CP
2. Spastic hemiplegia CP
3. Spastic quadriplegia CP
4. Athetoid CP
3
A newborn presents with prominent
hiccups,seizures and lethargy progressing to
coma
1. Nonketotic hyperglycenemia
2. Alexander disease
3. Maple syrup disease
4. Canavan disease
1
A 10 yr child with macrocephaly and
developmental delay and frontal region
changes in MRI suggests
1. Nonketotic hyperglycenemia
2. Alexander disease
3. Maple syrup disease
4. Canavan disease
2
A 10 yr child with seizures and developmental
delay and parietocccipital changes in MRI
suggests
1. X linked adrenoleucodystrophy
2. Alexander disease
3. Maple syrup disease
4. Canavan disease
1
Very long chain fatty acid is elevated and is
diagnostic in
1. X linked adrenoleucodystrophy
2. Alexander disease
3. Maple syrup disease
4. Canavan disease
1
Lorenzo oil is used in treatment of
1. X linked adrenoleucodystrophy
2. Alexander disease
3. Refsum Disease
4. Canavan disease
3
11yr child with suspected inborn error of
metabolism and hyperammonimia
1. X linked adrenoleucodystrophy
2. Maple syrup disease
3. Organic aciduria
4. Urea cycle defect
4
Drugs for treatment of partial seizures
1. Valproate
2. Carbamazepine
3. Phenytoin
4. Phenobarbitone
1
Recent
SSPE is diagnosed by all except
1. EEG
2. Brain biopsy
3. Antibody of measles in blood
4. Antibodies in CSF.
3
Cerebral palsy with most seizures is
1. Spastic diplegia CP
2. Spastic hemiplegia CP
3. Spastic quadriplegia CP
4. Athetoid CP
1
Swallowing develops at weeks of gestation
1. 10
2. 12
3. 14
4. 16
2
Recent asked
Eye lid opening at what gestational age
1. 24 week
2. 26
3. 28
4. 20
2
Prader willi syndrome is suspected in a floppy
infant and involved chromosome is
1. 10
2. 12
3. 15
4. 16
3
Angelman syndrome is suspected in a female
with over friendly and happy puppet face is
having chromosome involved
1. 10
2. 12
3. 15
4. 16
3
Thanks
N
Happy vacation

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Pediatric neurology mcq

  • 2. Boring topic that too in afternoon
  • 3. Waiting for the last slide
  • 4. For passing marks LP finding in APM and TBM Apm : very low glucose, neutrophilic, very high protein Tbm : low glucose, lymphocytic, high protein, cob web appearance
  • 5. Neurofibromatosis has all of the following except 1. Crowe sign 2. Lisch nodule 3. Brushfield iris 4. Neurofibroma 3
  • 6. Recent Tuberous sclerosis has all skin lesion except 1. Ash leaf macule 2. Adenoma sebacium 3. Shagreen patch 4. Angel kiss 4
  • 7. Reversible gallbaldder sludge detected by USG during treatment of bacterial meningitis is caused by 1. Ceftriaxone 2. Cefotaxime 3. Vancomycin 4. Meropenem 1
  • 8. Floppy baby Spinal muscular dystrophy important genetic cause of floppy baby invloves chromosome 1. 5 2. 6 3. 7 4. 9 1
  • 9. AFP Transverse myleitis involves mostly 1. Thoracic 2. Lumbar 3. Lumbosacral 4. Cervical 1 Afp causes are polio, gullian barre ,transverse myelitis, traumatic neuritis
  • 10. floppy Almond shaped eyes , with hyperphagia ,and obesity and hypogonadism and history of hypotonia in newborn period 1. Angelman 2. Prader willi 3. Gaucher 4. Tay Sach 2
  • 11. Anterior fontonalle closes at months 1. 2 -3 2. 4-7 3. 9-12 4. 18-24 4
  • 12. Total volume of CSF in neonate is 1. 50 ml 2. 100 ml 3. 25 ml 4. 150 ml 1 and 2 in adult
  • 13. Neural tube and neural migration Which of the following is neuronal migration defect 1. Shizencephaly 2. Myelomeningocele 3. SSPE 4. Gaucher 1
  • 14. True about hydranencephaly 1.Absent cerebral hemisphere 2. Sun setting sign 3.Mental retardation 4.Normal sized ventricle 1
  • 16. CSF production rate per hour is 1. 20 ml 2. 10 ml 3. 25 ml 4. 15 ml 1
  • 17. Normal ICP in a child is mmH20 1. 30 – 70 2. 50 – 80 3. 100 -150 4. 50 – 150 2 And 4 answer in case of adult
  • 18. Choose one 1. 3. 2. 4. All of the above
  • 19. Development Razing at what age 1. 4 m 2. 6 3. 8 4. 10 1
  • 20. Neck control at what age 1. 3 2. 6 3. 8 4. 10 1
  • 21. Recently asked 9 cube tower at what age month 1. 40 2. 30 3. 20 4. 15 Answer is 2. 2 cubes 15 month 4 cubes 18 month 6 cubes 22 month 7 cubes 24 9 cube 30 10 cube 36 month
  • 22. Casting at what age 1. 10 month 2. 6 3. 8 4. 12 4 casting means throwing things
  • 23. Mouthing and stranger anxiety and moros reflex should disapper at what age 1. 4 2. 6 3. 8 4. 10 2
  • 24. Object permenance, peek a boo game , waves bye bye , and immature pincer grasp at what age 1. 4 2. 6 3. 9 4. 10 3
  • 25. Separational anxiety, transitional object at what age 1. 12 2. 18 3. 15 4. 10 2
  • 26. 13yr old child presented with fever and altered sensorium with MRI shwoing medial temporal lobe involvement 1. HSV 2. Neisseria 3. Cerebral malaria 4. Fungal meningitis 1
  • 27. • Most common neurological sequele in bacterial meningitis 1.Recurrent seizures 2 Hearing loss 3 Cognitive loss 4 Visual loss 2
  • 28. Excessive irritability, crying,vomiting and difficulty feeding with history of frequent change in formula feeds suggests 1. Tay sach disease 2. Krabbes disease 3. Metachromatic leucodystrophy 4.Gaucher disease 2
  • 29. A child with painful acroparastheisa and angiokeratoma in skin with zebra bodies and maltese cross in urine sample suggests 1. Tay sach disease 2. Krabbes disease 3. Fabry disease 4.Gaucher disease 3
  • 30. Recent • Seizures with aphasia as abnormal finding is seen in 1. Absence seizures 2. West syndrome /Infantile spasm 3. Rolandic seizures 4. Landau klefner syndrome 4
  • 31. Recent • Hypsarrythmia is seen in 1. Absence seizures 2. West syndrome /Infantile spasm 3. Rolandic seizures 4. Landau klefner syndrome 2
  • 32. Recent • Periodic lateralised slowing in EEG is seen in 1. Absence seizures 2. Herpes simplex meningitis 3. Rolandic seizures 4. Landau klefner syndrome 2
  • 33. Recent • Multiple seizures of all types is seen in 1. Lennox gestaut syndrome 2. West syndrome /Infantile spasm 3. Rolandic seizures 4. Landau klefner syndrome 1
  • 34. Choose one 1. 3. 2. 4. All of the above
  • 35. Recent • Lafora disease has 1. Absence seizures 2. Infantile spasm 3. myoclonic seizures 4. GTCS 3
  • 36. Kernicterus in neonatal period is a major cause of 1. Spastic diplegia CP 2. Spastic hemiplegia CP 3. Spastic quadriplegia CP 4. Athetoid CP 4
  • 37. Most important risk factors for reurrence of febrile seizures is 1. Age < 2 yrs 2. Family History 3. Seizures at peak of fever 4. Long prolonged fever before seizure 2
  • 38. Passing mark q Cerebral palsy Cerebral palsy in which upper limb is more affected than lower limb is 1. Spastic diplegia CP 2. Spastic paraplegia CP 3. Spastic quadriplegia CP 4. Athetoid CP 1
  • 39. Prematurity is a major cause of 1. Spastic diplegia CP 2. Spastic hemiplegia CP 3. Spastic quadriplegia CP 4. Athetoid CP 1
  • 40. Birth asphyxia is a major cause of 1. Spastic diplegia CP 2. Spastic hemiplegia CP 3. Spastic quadriplegia CP 4. Athetoid CP 3
  • 41. A newborn presents with prominent hiccups,seizures and lethargy progressing to coma 1. Nonketotic hyperglycenemia 2. Alexander disease 3. Maple syrup disease 4. Canavan disease 1
  • 42. A 10 yr child with macrocephaly and developmental delay and frontal region changes in MRI suggests 1. Nonketotic hyperglycenemia 2. Alexander disease 3. Maple syrup disease 4. Canavan disease 2
  • 43. A 10 yr child with seizures and developmental delay and parietocccipital changes in MRI suggests 1. X linked adrenoleucodystrophy 2. Alexander disease 3. Maple syrup disease 4. Canavan disease 1
  • 44. Very long chain fatty acid is elevated and is diagnostic in 1. X linked adrenoleucodystrophy 2. Alexander disease 3. Maple syrup disease 4. Canavan disease 1
  • 45. Lorenzo oil is used in treatment of 1. X linked adrenoleucodystrophy 2. Alexander disease 3. Refsum Disease 4. Canavan disease 3
  • 46. 11yr child with suspected inborn error of metabolism and hyperammonimia 1. X linked adrenoleucodystrophy 2. Maple syrup disease 3. Organic aciduria 4. Urea cycle defect 4
  • 47. Drugs for treatment of partial seizures 1. Valproate 2. Carbamazepine 3. Phenytoin 4. Phenobarbitone 1
  • 48. Recent SSPE is diagnosed by all except 1. EEG 2. Brain biopsy 3. Antibody of measles in blood 4. Antibodies in CSF. 3
  • 49. Cerebral palsy with most seizures is 1. Spastic diplegia CP 2. Spastic hemiplegia CP 3. Spastic quadriplegia CP 4. Athetoid CP 1
  • 50. Swallowing develops at weeks of gestation 1. 10 2. 12 3. 14 4. 16 2
  • 51. Recent asked Eye lid opening at what gestational age 1. 24 week 2. 26 3. 28 4. 20 2
  • 52. Prader willi syndrome is suspected in a floppy infant and involved chromosome is 1. 10 2. 12 3. 15 4. 16 3
  • 53. Angelman syndrome is suspected in a female with over friendly and happy puppet face is having chromosome involved 1. 10 2. 12 3. 15 4. 16 3