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Article

Temporal bone abnormalities in children with GJB2 mutations.

The Laryngoscope - 1 Mar 2011

Kenna Margaret A, Rehm Heidi L, Frangulov Anna, Feldman Henry A, Robson Caroline D

Abstract excerpt

OBJECTIVES: To determine the incidence of temporal bone abnormalities in children with sensorineural hearing loss (SNHL) and pathogenic biallelic GJB2 mutations. STUDY DESIGN: Retrospective analysis of a large cohort of pediatric patients with biallelic GJB2 mutations and SNHL (observational case series). METHODS: Blinded review of all available temporal bone computed tomographic (CT) and magnetic resonance...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21298644
DOI: 10.1002/lary.21414
PMCID: PMC3061391

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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