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Cited 4 times in

A Case of Branchio-oculo-facial Syndrome.

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dc.contributor.authorPark, MY-
dc.contributor.authorKim, YC-
dc.date.accessioned2010-12-06T06:49:42Z-
dc.date.available2010-12-06T06:49:42Z-
dc.date.issued2009-
dc.identifier.issn1013-9087-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/438-
dc.description.abstractBranchio-oculo-facial syndrome (BOFS) is a rare, autosomal dominant disorder. It is characterized by distinct craniofacial abnormalities including abnormal location of the ears, aplastic cervical skin lesions, malformed auricles, conductive hearing loss, ocular abnormalities, and cleft lip and palate. Herein, we describe a case of BOFS with persistent aplasia cutis of the neck in a 5-year-old girl.-
dc.language.isoen-
dc.titleA Case of Branchio-oculo-facial Syndrome.-
dc.typeArticle-
dc.identifier.pmid20523806-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861242/-
dc.contributor.affiliatedAuthor김, 유찬-
dc.type.localJournal Papers-
dc.identifier.doi10.5021/ad.2009.21.3.288-
dc.citation.titleAnnals of dermatology-
dc.citation.volume21-
dc.citation.number3-
dc.citation.date2009-
dc.citation.startPage288-
dc.citation.endPage290-
dc.identifier.bibliographicCitationAnnals of dermatology, 21(3):288-290, 2009-
dc.identifier.eissn2005-3894-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Dermatology
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