Serum connexin 26 as a potential marker of non-syndromic hearing loss

Serum connexin 26 as a potential marker of non-syndromic hearing loss

Abstract Background Hearing loss (HL) represents the most common form of sensory impairment in both children and adults. In children, genetic causes account for over 50%. The genetic causes of HL include multiple syndromes associated with HL. In non-syndromic hearing loss (NSHL), patients have only...

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Bibliographic Details
Main Authors: Hend M. Moness, Noha M. Abdullah, Doaa El Amrousy, Reham Gamal, Hatem A. Mohamed, Mohammed A. Gomaa, Shaimaa Moustafa Hafez, Zamzam Hassan Mohamed
Format: Article
Language:English
Published: SpringerOpen 2025-01-01
Series:The Egyptian Journal of Otolaryngology
Subjects:
Connexin 26
ELISA
35delG
167delT
NSHL
Children
Online Access:https://doi.org/10.1186/s43163-025-00755-0
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