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Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss
The OTOA gene (Locus: DFNB22) is reported to be one of the causative genes for non-syndromic autosomal recessive hearing loss. The copy number variations (CNVs) identified in this gene are also known to cause hearing loss, but have not been identified in Japanese patients with hearing loss. Furtherm...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770988/ https://www.ncbi.nlm.nih.gov/pubmed/31527525 http://dx.doi.org/10.3390/genes10090715 |
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author | Sugiyama, Kenjiro Moteki, Hideaki Kitajiri, Shin-ichiro Kitano, Tomohiro Nishio, Shin-ya Yamaguchi, Tomomi Wakui, Keiko Abe, Satoko Ozaki, Akiko Motegi, Remi Matsui, Hirooki Teraoka, Masato Kobayashi, Yumiko Kosho, Tomoki Usami, Shin-ichi |
author_facet | Sugiyama, Kenjiro Moteki, Hideaki Kitajiri, Shin-ichiro Kitano, Tomohiro Nishio, Shin-ya Yamaguchi, Tomomi Wakui, Keiko Abe, Satoko Ozaki, Akiko Motegi, Remi Matsui, Hirooki Teraoka, Masato Kobayashi, Yumiko Kosho, Tomoki Usami, Shin-ichi |
author_sort | Sugiyama, Kenjiro |
collection | PubMed |
description | The OTOA gene (Locus: DFNB22) is reported to be one of the causative genes for non-syndromic autosomal recessive hearing loss. The copy number variations (CNVs) identified in this gene are also known to cause hearing loss, but have not been identified in Japanese patients with hearing loss. Furthermore, the clinical features of OTOA-associated hearing loss have not yet been clarified. In this study, we performed CNV analyses of a large Japanese hearing loss cohort, and identified CNVs in 234 of 2262 (10.3%, 234/2262) patients with autosomal recessive hearing loss. Among the identified CNVs, OTOA gene-related CNVs were the second most frequent (0.6%, 14/2262). Among the 14 cases, 2 individuals carried OTOA homozygous deletions, 4 carried heterozygous deletions with single nucleotide variants (SNVs) in another allele. Additionally, 1 individual with homozygous SNVs in the OTOA gene was also identified. Finally, we identified 7 probands with OTOA-associated hearing loss, so that its prevalence in Japanese patients with autosomal recessive hearing loss was calculated to be 0.3% (7/2262). As novel clinical features identified in this study, the audiometric configurations of patients with OTOA-associated hearing loss were found to be mid-frequency. This is the first study focused on the detailed clinical features of hearing loss caused by this gene mutation and/or gene deletion. |
format | Online Article Text |
id | pubmed-6770988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67709882019-10-30 Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss Sugiyama, Kenjiro Moteki, Hideaki Kitajiri, Shin-ichiro Kitano, Tomohiro Nishio, Shin-ya Yamaguchi, Tomomi Wakui, Keiko Abe, Satoko Ozaki, Akiko Motegi, Remi Matsui, Hirooki Teraoka, Masato Kobayashi, Yumiko Kosho, Tomoki Usami, Shin-ichi Genes (Basel) Article The OTOA gene (Locus: DFNB22) is reported to be one of the causative genes for non-syndromic autosomal recessive hearing loss. The copy number variations (CNVs) identified in this gene are also known to cause hearing loss, but have not been identified in Japanese patients with hearing loss. Furthermore, the clinical features of OTOA-associated hearing loss have not yet been clarified. In this study, we performed CNV analyses of a large Japanese hearing loss cohort, and identified CNVs in 234 of 2262 (10.3%, 234/2262) patients with autosomal recessive hearing loss. Among the identified CNVs, OTOA gene-related CNVs were the second most frequent (0.6%, 14/2262). Among the 14 cases, 2 individuals carried OTOA homozygous deletions, 4 carried heterozygous deletions with single nucleotide variants (SNVs) in another allele. Additionally, 1 individual with homozygous SNVs in the OTOA gene was also identified. Finally, we identified 7 probands with OTOA-associated hearing loss, so that its prevalence in Japanese patients with autosomal recessive hearing loss was calculated to be 0.3% (7/2262). As novel clinical features identified in this study, the audiometric configurations of patients with OTOA-associated hearing loss were found to be mid-frequency. This is the first study focused on the detailed clinical features of hearing loss caused by this gene mutation and/or gene deletion. MDPI 2019-09-16 /pmc/articles/PMC6770988/ /pubmed/31527525 http://dx.doi.org/10.3390/genes10090715 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sugiyama, Kenjiro Moteki, Hideaki Kitajiri, Shin-ichiro Kitano, Tomohiro Nishio, Shin-ya Yamaguchi, Tomomi Wakui, Keiko Abe, Satoko Ozaki, Akiko Motegi, Remi Matsui, Hirooki Teraoka, Masato Kobayashi, Yumiko Kosho, Tomoki Usami, Shin-ichi Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title | Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title_full | Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title_fullStr | Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title_full_unstemmed | Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title_short | Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss |
title_sort | mid-frequency hearing loss is characteristic clinical feature of otoa-associated hearing loss |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770988/ https://www.ncbi.nlm.nih.gov/pubmed/31527525 http://dx.doi.org/10.3390/genes10090715 |
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