지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2013.1
- 수록면
- 594 - 598 (5page)
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초록· 키워드
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Among 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.
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등록된 정보가 없습니다.
참고문헌 (14)
참고문헌 신청
Cohen NL / 2004 / Meningitis in cochlear implant recipients: the North American experience / Otol Neurotol 25 (3) : 275 ~ 281
Cremers CW / 1983 / Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery) / Int J Pediatr Otorhi
Incesulu A / 2008 / Cochlear implantation in cases with incomplete partition type III (X-linked anomaly) / Eur Arch Otorhinolaryngol 265 (11) : 1425 ~ 1430
Jackler RK / 1987 / Congenital malformations of the inner ear: a classification based on embryogenesis / Laryngoscope 97 (3 Pt 2 Suppl 40) : 2 ~ 14
Lee HK / 2009 / Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants / Clin Genet 75 (6) : 572 ~ 575
Cremers CW / 1983 / Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery) / Int J Pediatr Otorhi
Incesulu A / 2008 / Cochlear implantation in cases with incomplete partition type III (X-linked anomaly) / Eur Arch Otorhinolaryngol 265 (11) : 1425 ~ 1430
Jackler RK / 1987 / Congenital malformations of the inner ear: a classification based on embryogenesis / Laryngoscope 97 (3 Pt 2 Suppl 40) : 2 ~ 14
Lee HK / 2009 / Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants / Clin Genet 75 (6) : 572 ~ 575
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