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Article

[Keratitis-ichthyosis-deafness (KID) syndrome].

Annales de dermatologie et de venereologie - 1 Jan 2008

Mazereeuw-Hautier J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18342082
DOI: 10.1016/j.annder.2007.11.013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Genotype-Phenotype Correlations, Mortality, and Clinical Insights in Keratitis-Ichthyosis-Deafness Syndrome: A Comprehensive Review and Case Report.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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