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Crouzon 증후군 환자의 증례보고

DC Field Value Language
dc.contributor.author이수진-
dc.contributor.author김영재-
dc.contributor.author장기택-
dc.contributor.author이상훈-
dc.contributor.author김종철-
dc.contributor.author한세현-
dc.contributor.author김정욱-
dc.date.accessioned2010-02-01T09:58:12Z-
dc.date.available2010-02-01T09:58:12Z-
dc.date.issued2009-
dc.identifier.citation대한소아치과학회지, 36:133-138, 2009.en
dc.identifier.issn1226-8496-
dc.identifier.urihttps://hdl.handle.net/10371/47935-
dc.description.abstractCrouzon 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.isokoen
dc.publisher대한소아치과학회en
dc.subjectCrouzon syndromeen
dc.subjectCraniosynostosisen
dc.subjectMaxillary hypoplasiaen
dc.subjectHypertelorismen
dc.subjectExophthalmosen
dc.titleCrouzon 증후군 환자의 증례보고en
dc.typeArticleen
dc.contributor.AlternativeAuthorLee, Su-Jin-
dc.contributor.AlternativeAuthorKim, Young-Jae-
dc.contributor.AlternativeAuthorLee, Sang-Hoon-
dc.contributor.AlternativeAuthorJang, Ki-Taek-
dc.contributor.AlternativeAuthorKim, Chong-Chul-
dc.contributor.AlternativeAuthorHahn, Se-Hyun-
dc.contributor.AlternativeAuthorKim, Jung-Wook-
Appears in Collections:
College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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