Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China

ObjectiveThis study aimed to delineate the prevalence and mutation spectrum of deafness-associated genes among newborns in a resource-limited region of China, and to assess the diagnostic yield of combined hearing and genetic screening.MethodsFrom May 2017 to May 2023, 22,819 newborns underwent conc...

Descrizione completa

Dettagli Bibliografici

Autori principali:	Qin She, Hui-Lin Ou, Er-Fang Tang, Wei Huang, Wei-He Tan, Mu-Lan Zeng, Xiu-Feng Pan, Chen-Bing Liu
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Frontiers Media S.A. 2026-06-01
Serie:	Frontiers in Genetics
Soggetti:	genetic screening for deafness GJB2 gene mutations neonatal hearing screening resource-limited regions whole exome sequencing (WES)
Accesso online:	https://www.frontiersin.org/articles/10.3389/fgene.2026.1873535/full
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!