scholarly journals Differences and similarities of cochlear and vestibular endorgans in patients with hereditary hearing loss

2018 ◽  
Vol 77 (3) ◽  
pp. 180-187
Author(s):  
Keita Tsukada ◽  
Shin-ichi Usami
Keyword(s):  
Hearing Loss ◽  
Hereditary Hearing Loss ◽  
Vestibular Endorgans

scholarly journals Gene Expression Profiles of the Cochlea and Vestibular Endorgans

2015 ◽  
Vol 124 (1_suppl) ◽  
pp. 6S-48S ◽  
Author(s):  
Shin-ya Nishio ◽  
Mitsuru Hattori ◽  
Hideaki Moteki ◽  
Keita Tsukada ◽  
Maiko Miyagawa ◽  
...  
Keyword(s):  
Gene Expression ◽  
Hearing Loss ◽  
Expression Profiles ◽  
Expression Patterns ◽  
Gene Expression Profiles ◽  
Vestibular Function ◽  
Specific Expression ◽  
Hereditary Hearing Loss ◽  
Vestibular Endorgans ◽  
Gene Symbols

Objectives:We sought to elucidate the gene expression profiles of the causative genes as well as the localization of the encoded proteins involved in hereditary hearing loss.Methods:Relevant articles (as of September 2014) were searched in PubMed databases, and the gene symbols of the genes reported to be associated with deafness were located on the Hereditary Hearing Loss Homepage using localization, expression, and distribution as keywords.Results:Our review of the literature allowed us to systematize the gene expression profiles for genetic deafness in the inner ear, clarifying the unique functions and specific expression patterns of these genes in the cochlea and vestibular endorgans.Conclusions:The coordinated actions of various encoded molecules are essential for the normal development and maintenance of auditory and vestibular function.

Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries

2021 ◽  
Author(s):  
Abdullah Al Mutery ◽  
Mona Mahfood ◽  
Jihen Chouchen ◽  
Abdelaziz Tlili
Keyword(s):  
Hearing Loss ◽  
Gulf Cooperation Council ◽  
Genetic Etiology ◽  
Hereditary Hearing Loss

scholarly journals Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population

2015 ◽  
Vol 60 (10) ◽  
pp. 613-617 ◽  
Author(s):  
Mirei Taniguchi ◽  
Hirotaka Matsuo ◽  
Seiko Shimizu ◽  
Akiyoshi Nakayama ◽  
Koji Suzuki ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Carrier Frequency ◽  
Japanese Population ◽  
Hereditary Hearing Loss ◽  
Gjb2 Mutations

scholarly journals Perda auditiva genética

2003 ◽  
Vol 69 (1) ◽  
pp. 100-104 ◽  
Author(s):  
Ricardo Godinho ◽  
Ivan Keogh ◽  
Roland Eavey
Keyword(s):  
Hearing Loss ◽  
Home Page ◽  
Hereditary Hearing Loss

O progresso das pesquisas relacionadas à perda auditiva genética tem provocado um importante avanço do entendimento dos mecanismos moleculares que governam o desenvolvimento, a função, a resposta ao trauma e o envelhecimento do ouvido interno. Em países desenvolvidos, mais de 50% dos casos de surdez na infância é causada por alterações genéticas e as perdas auditivas relacionadas à idade têm sido associadas com mecanismos genéticos. OBJETIVO: O objetivo desta revisão é relatar as informações mais recentes relacionadas às perdas audtivas de origem genética. FORAMA DE ESTUDO: Revisão sistemática. MATERIAL E MÉTODO: A revisão da literatura inclui artigos indexados à MEDLINE (Biblioteca Nacional de Saúde, NIH-USA) e publicados nos últimos 3 anos, além das informações disponíveis na Hereditary Hearing Loss Home Page. CONCLUSÃO: Os recentes avanços no entendimento das perdas auditivas de origem genética têm favorecido a nossa compreensão da função auditiva e tornado o diagnóstico mais apurado. Possivelmente, no futuro, este conhecimento também proporcionará o desenvolvimento de novas terapias para o tratamento das causas genéticas das perdas auditivas.

Hereditary Hearing Loss with Thyroid Abnormalities

2011 ◽  
pp. 43-49 ◽  
Author(s):  
Byung Yoon Choi ◽  
Julie Muskett ◽  
Kelly A. King ◽  
Christopher K. Zalewski ◽  
Thomas Shawker ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Hereditary Hearing Loss ◽  
Thyroid Abnormalities
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