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Comprehensive clinical and genetic profiling of Vietnamese pediatric hearing loss: a multi-region exome sequencing study.

Human molecular genetics - 23 Mar 2026

Hoang Nguyen Cong, Nguyen-Le Duc-Minh, Tran Huyen-Trang Thi, Nguyen Thanh Tra, Nguyen Manh Hung, Ngo Dai-Phu, Le Giau, Van-Ho Hoang-Kim, Ha Gia Huy, Anh Tran Trung, Hoang Viet, Lan Le Thi Huong, Tuan Nguyen Minh, Nguyet Dao Minh, Giang Bui Bang, Thanh Le Dinh, Nguyen Phu Hung, Luu Phuc-Loi

Abstract excerpt

Congenital hearing loss (HL) in the Vietnamese population remains understudied despite its genetic diversity, limiting our understanding of its genetic etiology and hindering the development of effective, population-specific diagnostic strategies. In this descriptive cross-sectional whole-exome sequencing study, we enrolled 150 children with congenital non-syndromic HL (NSHL) from hospitals and hearing centers...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 41955303
DOI: 10.1093/hmg/ddag027

Genes

GJB2
MAF
MYO6
COCH

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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