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Article

[Patient with severe corneal disease in KID syndrome].

Archivos de la Sociedad Espanola de Oftalmologia - 1 Apr 2006

Gómez-Faiña P, Ruiz-Viñals A T, Buil-Calvo J A, España-Albelda A, Pazos-López M, Castilla-Céspedes M

Abstract excerpt

CASE REPORT: A 33-year-old woman with superficial and deep bilateral corneal vascularization and keratoconjunctivitis sicca, keratoerythema and neurosensory deafness, was diagnosed with keratitis-ichthyosis-deafness (KID) syndrome. DISCUSSION: KID syndrome is a congenital ectodermal dysplasia characterized by the association of vascularizing keratitis, hyperkeratotic skin lesions and sensorineural hearing loss....

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Source

Identifiers

PMID: 16688648
DOI: 10.4321/s0365-66912006000400010

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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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[Patient with severe corneal disease in KID syndrome].PMID 16688648Read ↗

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Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndrome.Semantic proximity Read ↗

[Keratitis-ichthyosis-deafness (KID) syndrome: an observation in a child in sub-Saharan Africa].Semantic proximity Read ↗

Severe Phenotype of Keratitis-Ichthyosis-Deafness Syndrome With Presumed Ocular Surface Squamous Neoplasia.Semantic proximity Read ↗

GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form.Semantic proximity Read ↗

[Connexin 26 mutation and keratitis-ichthyosis-deafness (KID) syndrome].Semantic proximity Read ↗

KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation.Semantic proximity Read ↗

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 ↗

Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.Semantic proximity Read ↗

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