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Sindrome de crouzon
- 1. María Camila Naranjo Hurtado Once B code: 20
- 2. “DISOSTOSIS CRANEOFACIAL CONGÉNITA”, IT'S BEGINNING IS GENETIC. IS CHARACTERIZED BY DEFORMITYS IN THE CRANIUM AND THE FACE. IT IS AN UPSET. CAUSES A MERGER FOR THE BONES. WHEN THE STRUCTURES BIND FAST THE CRANIUM THEY GROW IN COURSE OF THE OPEN STRUCTURES.
- 3. • IS GENETIC • MUTATION OF THE FGFR2 (receptor of development receptor) OR THE FGFR3 • A MUTATION IN THIS GENE(s),IT CAUSES THAT THE BONES BIND EARLY BASICALLY THE DOCTORS CONTINUE STUDYING THIS ILLNESS BECAUSE IS SO STRANGE
- 4. • PARENTS THAT HAVE THE UPSET • PARENTS THAT DONT HAVE THE UPSET BUT CARRY THE GEN • PARENTS TO HACE AN ADVANCED AGE
- 5. THE MAIN SIGN AND SYMPTOMS ARE: 1. THE UPPER AND LOWER PART OF THE HEAD ARE CRUSH 2. THE NOSE IS SIMILAR TO A PICK 3. THE LOWER JAW IS BIG AND PROTRUDING 4. MISALIGNED TEETH 5. TIGHT PALATE AND CRACK 6. LOSE THE AUDITION 7. THE EARS ARE DEFORMITYS 8. VISION PROBLEMS
- 6. 1. CURVATURE FOR THE SPINE 2. HEADACHE
- 7. THE DOCTORS ARE ABLE TO DIAGNOSE THIS UPSET IN THE CHILDHOOD . OR CAN MAKE EXAMS AS: X RAYS GENETIC TESTINGS TAKE IMAGES FOR THE STRUCTURE OF THE BODY
- 8. FOR CROUZON UNKNOW A TREARTMENT BECAUSE THE DOCTORS DONT KNOW THE MOLECULAR CAUSE FOR THIS GENES BUT EXIST OPTIONS LIKE A: SURGERY CRANIECTOMY SURGERY TO THEAT EXOPHTHALMOS: • in the eyes SURGERY TO REPAIR THE PROTRUNDING JAW ORTHODONTIC TREATMENT OCULAR AND HEARING TREATMENT
- 9. I THINK THAT EVERYBODY MUST CARE THEMSELFS, WHEN SOMEBODY TAKE THE DECISION TO HAVE CHILDRENS, MUST INVESTIGATE ABOUT HIS BODY, AND PREVENT ANY ILLNESS.
- 10. 1. MERGER: FUSION 2. BIND: COMBINAR 3. UPSET: MALESTAR 4. CRUSH: APLASTADO 5. PICK: PICO 6. JAW: MANDIBULA 7. PROTRUNDING: PROTUBERANTE 8. MISALINGNED: DESALINEADA 9. TIGHT: ESTRECHO 10. CRACK: HENDIDO 11. HEADACHE: DOLOR DE CABEZA 12. CRANIECTOMY: CRANIECTOMIA 13. EXOPHTHALMOS: EXOLFTAMIA