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Article

Causes of hearing impairment in the Norwegian paediatric cochlear implant program.

International journal of audiology - 1 Aug 2010

Siem Geir, Fagerheim Toril, Jonsrud Christoffer, Laurent Claude, Teig Erik, Harris Sten, Leren Trond P, Früh Andreas, Heimdal Ketil

Abstract excerpt

Severe to profound hearing impairment (HI) is estimated to affect around 1/2000 young children. Advances in genetics have made it possible to identify several genes related to HI. This information can cast light upon prognostic factors regarding the outcome in cochlear implantation, and provide information both for scientific and genetic counselling purposes. From 1992 to 2005, 273 children from 254 families...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20553101
DOI: 10.3109/14992021003743269

Genes

GJB2
GJB6
KCNQ1

Variants

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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