Literature DB >> 29089220

[Genetic hearing loss].

Lei Tanaka-Ouyang1, Sandrine Marlin2, Jérôme Nevoux3.   

Abstract

Deafness is the most common sensory disability in developed countries affecting more than 2 births in 1000. Eighty percent of congenital deafness is genetic. Universal newborn hearing screening has been in place since 2012 in France. All genetic hearing losses are not congenital and all congenital hearing losses are not genetic. Genetic hearing loss may be syndromic (associated with other symptoms) (10 %) or non-syndromic (isolated) (90 %). Hearing loss may initially be the only symptom of syndromic deafness. A genetic origin can be diagnosed and must therefore be evoked systematically even in the adult.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

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Year:  2017        PMID: 29089220     DOI: 10.1016/j.lpm.2017.09.005

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  2 in total

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Authors:  Anaïs Le Nabec; Mégane Collobert; Cédric Le Maréchal; Rémi Marianowski; Claude Férec; Stéphanie Moisan
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2.  3D Chromatin Organization Involving MEIS1 Factor in the cis-Regulatory Landscape of GJB2.

Authors:  Anaïs Le Nabec; Clara Blotas; Alinéor Briset; Mégane Collobert; Claude Férec; Stéphanie Moisan
Journal:  Int J Mol Sci       Date:  2022-06-23       Impact factor: 6.208

  2 in total

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