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Article

Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center.

PloS one - 1 Jan 2011

Wu Chen-Chi, Hung Chia-Cheng, Lin Shin-Yu, Hsieh Wu-Shiun, Tsao Po-Nien, Lee Chien-Nan, Su Yi-Ning, Hsu Chuan-Jen

Abstract excerpt

Universal newborn hearing screening (UNHS) is of paramount importance for early identification and management of hearing impairment in children. However, infants with slight/mild, progressive, or late-onset hearing impairment might be missed in conventional UNHS. To investigate whether genetic screening for common deafness-associated mutations could assist in identifying these infants, 1017 consecutive newborns...

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Identifiers

PMID: 21811586
DOI: 10.1371/journal.pone.0022314
PMCID: PMC3139636

Genes

GJB2
NHS

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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