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불완전 분할 3형 내이기형 환자에서 시행한 인공와우 이식술 1예

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dc.contributor.author반명진-
dc.date.accessioned2021-08-12T00:46:26Z-
dc.date.available2021-08-12T00:46:26Z-
dc.date.created2021-06-17-
dc.date.issued2013-09-
dc.identifier.issn2092-5859-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/13381-
dc.description.abstractAmong the inner ear anomalies, incomplete partition type III (IP III) is a rare finding. The X-linked deafness type 3 (DFN3), the most common type of X-linked hearing loss of its kind, results from mutations in the POU3F4 gene and accounts for -50% of all families carrying X-linked non-syndromic hearing loss. Pathognomonic temporal bone deformities, recently classified as IP III, have been associated with DFN3. We report a patient with IP III carrying a mutation in the POU3F4 gene who experienced cerebrospinal fluid gusher during and after cochlear implantation.-
dc.language한국어-
dc.language.isoko-
dc.publisher대한이비인후과학회-
dc.title불완전 분할 3형 내이기형 환자에서 시행한 인공와우 이식술 1예-
dc.title.alternativeA Case of Cochlear Implantation in Patient with Incomplete Partition Type III Inner Ear Anomaly-
dc.typeArticle-
dc.contributor.affiliatedAuthor반명진-
dc.identifier.bibliographicCitation대한이비인후과학회지 두경부외과학, v.56, no.9, pp.594 - 598-
dc.relation.isPartOf대한이비인후과학회지 두경부외과학-
dc.citation.title대한이비인후과학회지 두경부외과학-
dc.citation.volume56-
dc.citation.number9-
dc.citation.startPage594-
dc.citation.endPage598-
dc.type.rimsART-
dc.description.journalClass2-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorincomplete partition type III-
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