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Cochlear implantation in the patients with CDH23 mutations Maiko Miyagawa 1 1Department of Otolaryngology,Shinshu University School of Medicine pp.59-63
Published Date 2012/1/20
DOI https://doi.org/10.11477/mf.1411102047
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 Mutations in the CDH23 gene are known to be responsible for both Usher syndrome type ID(USH1D)and non-syndromic hearing loss(DFNB12),and molecular confirmation has become important in the diagnosis of these conditions. Hearing loss of the patients with CDH23 mutations is congenital or early onset,progressive high frequency involved hearing loss. With regard to the intervention of the patients with CDH23 mutations,no detailed study has been published. In the present paper,we reported three patients received cochlear implantation and showed good performance after implantation. We concluded that cochlear implantation is a good therapeutic intervention for the patients with CDH23 mutations.


Copyright © 2012, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1316 印刷版ISSN 0914-3491 医学書院

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