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Crouzon 증후군 환자의 증례보고
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이수진 | - |
dc.contributor.author | 김영재 | - |
dc.contributor.author | 장기택 | - |
dc.contributor.author | 이상훈 | - |
dc.contributor.author | 김종철 | - |
dc.contributor.author | 한세현 | - |
dc.contributor.author | 김정욱 | - |
dc.date.accessioned | 2010-02-01T09:58:12Z | - |
dc.date.available | 2010-02-01T09:58:12Z | - |
dc.date.issued | 2009 | - |
dc.identifier.citation | 대한소아치과학회지, 36:133-138, 2009. | en |
dc.identifier.issn | 1226-8496 | - |
dc.identifier.uri | https://hdl.handle.net/10371/47935 | - |
dc.description.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. | en |
dc.language.iso | ko | en |
dc.publisher | 대한소아치과학회 | en |
dc.subject | Crouzon syndrome | en |
dc.subject | Craniosynostosis | en |
dc.subject | Maxillary hypoplasia | en |
dc.subject | Hypertelorism | en |
dc.subject | Exophthalmos | en |
dc.title | Crouzon 증후군 환자의 증례보고 | en |
dc.type | Article | en |
dc.contributor.AlternativeAuthor | Lee, Su-Jin | - |
dc.contributor.AlternativeAuthor | Kim, Young-Jae | - |
dc.contributor.AlternativeAuthor | Lee, Sang-Hoon | - |
dc.contributor.AlternativeAuthor | Jang, Ki-Taek | - |
dc.contributor.AlternativeAuthor | Kim, Chong-Chul | - |
dc.contributor.AlternativeAuthor | Hahn, Se-Hyun | - |
dc.contributor.AlternativeAuthor | Kim, Jung-Wook | - |
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