Spectrum of genetic variants in bilateral sensorineural hearing loss

Spectrum of genetic variants in bilateral sensorineural hearing loss

Background: Hearing loss (HL) is an impairment of auditory function with identified genetic forms that can be syndromic (30%) or non-syndromic (70%). HL is genetically heterogeneous, with more than 1,000 variants across 150 causative genes identified to date. The genetic diagnostic rate varies signi...

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Bibliographic Details
Main Authors: Amanat Ali, Mohammed Tabouni, Praseetha Kizhakkedath, Ibrahim Baydoun, Mushal Allam, Anne John, Faiza Busafared, Ayesha Alnuaimi, Fatma Al-Jasmi, Hiba Alblooshi
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-02-01
Series:Frontiers in Genetics
Subjects:
bilateral sensorineural hearing loss
genetic variants
MYO15A gene
SLC26A4 gene
GJB2 gene
CDH23 gene
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2024.1314535/full

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https://www.frontiersin.org/articles/10.3389/fgene.2024.1314535/full

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