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
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.
