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Article

Cochlear implantation in keratitis-ichthyosis-deafness syndrome: 10-year follow-up of two patients.

Cochlear implants international - 1 Feb 2012

Smyth C M, Sinnathuray A R, Hughes A E, Toner J G

Abstract excerpt

OBJECTIVE AND IMPORTANCE: The objective of this study was to describe long-term outcomes after cochlear implantation in keratitis-ichthyosis-deafness (KID) syndrome, often caused by GJB2 mutations, in the context of other reported cases. Clinical presentation and intervention: The authors conducted correlative clinical and molecular genetic analysis on two implanted patients with KID syndrome, and tabulated...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22340753
DOI: 10.1179/146701011X12950038111936

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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Cochlear implantation in keratitis-ichthyosis-deafness syndrome: 10-year follow-up of two patients.PMID 22340753Read ↗

A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.Semantic proximity Read ↗

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Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report.Semantic proximity Read ↗

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