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The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome
Objectives. This study aimed to determine the feasibility of cochlear implantation for sensorineural hearing loss in patients with Waardenburg syndrome. Method. A retrospective chart review was performed on patients who underwent cochlear implantation at the University of Tokyo Hospital. Clinical cl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916269/ https://www.ncbi.nlm.nih.gov/pubmed/27376080 http://dx.doi.org/10.1155/2016/2854736 |
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author | Koyama, Hajime Kashio, Akinori Sakata, Aki Tsutsumiuchi, Katsuhiro Matsumoto, Yu Karino, Shotaro Kakigi, Akinobu Iwasaki, Shinichi Yamasoba, Tatsuya |
author_facet | Koyama, Hajime Kashio, Akinori Sakata, Aki Tsutsumiuchi, Katsuhiro Matsumoto, Yu Karino, Shotaro Kakigi, Akinobu Iwasaki, Shinichi Yamasoba, Tatsuya |
author_sort | Koyama, Hajime |
collection | PubMed |
description | Objectives. This study aimed to determine the feasibility of cochlear implantation for sensorineural hearing loss in patients with Waardenburg syndrome. Method. A retrospective chart review was performed on patients who underwent cochlear implantation at the University of Tokyo Hospital. Clinical classification, genetic mutation, clinical course, preoperative hearing threshold, high-resolution computed tomography of the temporal bone, and postoperative hearing outcome were assessed. Result. Five children with Waardenburg syndrome underwent cochlear implantation. The average age at implantation was 2 years 11 months (ranging from 1 year 9 months to 6 years 3 months). Four patients had congenital profound hearing loss and one patient had progressive hearing loss. Two patients had an inner ear malformation of cochlear incomplete partition type 2. No surgical complication or difficulty was seen in any patient. All patients showed good hearing outcome postoperatively. Conclusion. Cochlear implantation could be a good treatment option for Waardenburg syndrome. |
format | Online Article Text |
id | pubmed-4916269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49162692016-07-03 The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome Koyama, Hajime Kashio, Akinori Sakata, Aki Tsutsumiuchi, Katsuhiro Matsumoto, Yu Karino, Shotaro Kakigi, Akinobu Iwasaki, Shinichi Yamasoba, Tatsuya Biomed Res Int Research Article Objectives. This study aimed to determine the feasibility of cochlear implantation for sensorineural hearing loss in patients with Waardenburg syndrome. Method. A retrospective chart review was performed on patients who underwent cochlear implantation at the University of Tokyo Hospital. Clinical classification, genetic mutation, clinical course, preoperative hearing threshold, high-resolution computed tomography of the temporal bone, and postoperative hearing outcome were assessed. Result. Five children with Waardenburg syndrome underwent cochlear implantation. The average age at implantation was 2 years 11 months (ranging from 1 year 9 months to 6 years 3 months). Four patients had congenital profound hearing loss and one patient had progressive hearing loss. Two patients had an inner ear malformation of cochlear incomplete partition type 2. No surgical complication or difficulty was seen in any patient. All patients showed good hearing outcome postoperatively. Conclusion. Cochlear implantation could be a good treatment option for Waardenburg syndrome. Hindawi Publishing Corporation 2016 2016-06-08 /pmc/articles/PMC4916269/ /pubmed/27376080 http://dx.doi.org/10.1155/2016/2854736 Text en Copyright © 2016 Hajime Koyama et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Koyama, Hajime Kashio, Akinori Sakata, Aki Tsutsumiuchi, Katsuhiro Matsumoto, Yu Karino, Shotaro Kakigi, Akinobu Iwasaki, Shinichi Yamasoba, Tatsuya The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title | The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title_full | The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title_fullStr | The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title_full_unstemmed | The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title_short | The Hearing Outcomes of Cochlear Implantation in Waardenburg Syndrome |
title_sort | hearing outcomes of cochlear implantation in waardenburg syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916269/ https://www.ncbi.nlm.nih.gov/pubmed/27376080 http://dx.doi.org/10.1155/2016/2854736 |
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