The Crouzan Syndrome-A Case Report Key Words: Craniofacial syndromes, Crouzon syndrome, Premature synostosis
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کرانیوفاسیال دیسوستوزیس و گزارش یک مورد جراحی سندرم کروزون
The most important craniofacial dysostosis & syndromes are Crouzon, Apret, Pfeiffer.Carpenter Saether- Chotzen. The common characteristic is premature closure of cranial sutures, which result in Maxillofacial deformities. Perfect recognition and carefully evaluation are the most important points in their reconstruction surgery.Because the prevalence & surgical treatment of Crouzon syndrome is l...
متن کاملPremature Craniosynostosis in a Rare Genetic Disease- A Case Report
BACKGROUND Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity. Its most notable characteristic feature is premature synostosis of cranial sutures The case presented is of a 4 yr old boy with box like head with microcephaly, protuberant eyes, hydrocephalus, low visual acquity diagnosed as a case of crouzon syndr...
متن کاملEarly orthodontic management of Crouzon Syndrome: a case report.
Crouzon Syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the first year of life...
متن کاملCrouzon Syndrome: a case report
Crouzon Syndrome is a rare genetic disorder resulting from a mutation of the Fibroblast Growth Factor Receptor 2 Gene. The main presenting feature of this syndrome is craniofacial synostosis but multiple physical dysmorphic features have been reported. There is a dearth of literature detailing the presentation of this syndrome in the foot and lower limb. Therefore, this case report will describ...
متن کاملLETTER TO JMG Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
C raniosynostosis, the premature fusion of one or more sutures of the skull, is a common craniofacial anomaly, with an estimated incidence of 1/2000 to 1/3000 births. 2 Characteristic deformities of skull shape occur as a result of different patterns of sutural fusion, while compensatory skull expansion occurs at unaffected sutures to accommodate the growing brain. Premature fusion of the sagit...
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تاریخ انتشار 2013