منابع مشابه
Crouzon 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 کاملCrouzon syndrome - A rare case report
Crouzon syndrome is the most common syndrome among the craniosynostosis group. Crouzon syndrome accounts for about 4.8% of all of them. It commonly has autosomal dominant inheritance with complete penetrance and variable expressivity from subtle to severe forms and characterized by craniosynostosis, exophthalmos, and hypoplastic maxilla with relative mandibular prognathism. Mutation of the fibr...
متن کاملCrouzon syndrome in association with acanthosis nigricans
Crouzon syndrome is a rare inherited autosomal dominant syndrome characterized by craniosynostosis, midface hypoplasia. Acanthosis nigricans may be associated with Crouzon syndrome, but it differs from the classic crouzon syndrome. This is a report of a 30-year-old-woman who presented acanthosis nigricans coexist with crouzon syndrome.
متن کامل"Spectaclesplasty" periorbital rotation advancement in Crouzon syndrome.
Facial deformity in Crouzon syndrome is characterized by exophthalmos, exorbitism, mild hypertelorism, and maxillary hypoplasia with a Class III occlusion. The Göteborg craniofacial unit corrects this deformity in selected patients by the 2-stage procedure of "spectaclesplasty" followed by a Le Fort I maxillary osteotomy at skeletal maturity. "Spectacles" is a reference to the bilateral circumf...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2012
ISSN: 1757-790X
DOI: 10.1136/bcr-2012-007242