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

Annales de dermatologie et de venereologie - 1 May 2011

Barruet K, Saka B, Kombaté K, Mouhari-Toure A, Nguepmeni Noune J, Akakpo S, Tchangaï-Walla K, Pitché P

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Identifiers

PMID: 21570577
DOI: 10.1016/j.annder.2011.02.006

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[Keratitis-ichthyosis-deafness (KID) syndrome: an observation in a child in sub-Saharan Africa].PMID 21570577Read ↗

[Keratitis-ichthyosis-deafness (KID) syndrome].Semantic proximity Read ↗

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

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Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome.Semantic proximity Read ↗

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Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation.Semantic proximity Read ↗

Keratitis-ichthyosis-deafness syndrome with lethal p.Ala88Val variant and severe hypercalcemia.Semantic proximity Read ↗

A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E.Semantic proximity Read ↗

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

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

[Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children].Semantic proximity Read ↗

From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.Semantic proximity Read ↗

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