Analysis of mitochondrial 12S rRNA A1555G genetic mutation in group of Egyptian children with non-syndromic hearing loss: cross-sectional observational study

Analysis of mitochondrial 12S rRNA A1555G genetic mutation in group of Egyptian children with non-syndromic hearing loss: cross-sectional observational study

Abstract Background Hearing loss is a multifactorial condition with the etiology of hereditary and/or environmental factors, which leads to various degrees of hearing impairment. One of the most common mutations associated with aminoglycoside-induced non-syndromic hearing impairment in the mitochond...

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Bibliographic Details
Main Authors: Hala M. Zeidan, Heba Tallah Sherif Abd El Hady, Abir Omara, Nagwa A. Meguid, Mohamed S. Taha
Format: Article
Language:English
Published: SpringerOpen 2025-05-01
Series:The Egyptian Journal of Otolaryngology
Subjects:
Hearing loss
Non-syndromic
Mitochondrial mutations
A1555G
Egypt
Online Access:https://doi.org/10.1186/s43163-025-00839-x
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https://doi.org/10.1186/s43163-025-00839-x

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