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Article

Two Cases of Chronic Candidiasis in Keratitis-Ichthyosis-Deafness Syndrome.

The American Journal of dermatopathology - 1 Oct 2018

Bartenstein Diana, Chung Hye Jin, Hussain Sadaf

Abstract excerpt

Keratitis-ichthyosis-deafness (KID) syndrome is a rare genodermatosis that typically results from mutations of the GJB2 gene or, less commonly, the GJB6 gene. Patients with KID syndrome are at higher risk of malignancy and infections. Here, we present 2 patients with KID syndrome who developed verrucous plaques. Given that patients with KID syndrome are at high risk of developing squamous cell carcinoma, biopsies...

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Source

Identifiers

PMID: 29742560
DOI: 10.1097/DAD.0000000000001178

Genes

GJB2
GJB6

Provenance

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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