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Crouzon 증후군 환자의 증례보고

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Authors
이수진; 김영재; 장기택; 이상훈; 김종철; 한세현; 김정욱
Issue Date
2009
Publisher
대한소아치과학회
Citation
대한소아치과학회지, 36:133-138, 2009.
Keywords
Crouzon syndromeCraniosynostosisMaxillary hypoplasiaHypertelorismExophthalmos
Abstract
Crouzon syndrome is a rare disease, first decribed by Crouzon in 1912. This syndrome is cuased by mutations in the FGFR2 gene, which is mapped to chromosome locus 10q25-10q26. The condition occurs in about 1 of every 25,000 birth and is inherited as an autosomal dominant trait. We experienced a case of Crouzon's disease in a 9-year-old-female child. Physical examination revealed craniosynostosis, hypertelorism, exophthalmos, hypoplastic maxilla and a relative mandibular prognathism. The purpose of this study is to report the dental and medical characteristics of the patient and review the literatures of Crouzon syndrome.
ISSN
1226-8496
Language
Korean
URI
https://hdl.handle.net/10371/47935
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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