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hyperkeratóza epidermolytická

  1. Subject h.hyperkeratóza epidermolytická
    Subject h.Hyperkeratosis, Epidermolytic
    Entry termserytroderma ichtyoziformná bulózna
    erytroderma ichtyoziformná bulózna vrodená
    erytroderma ichtyoziformná bulózna kongenitálna
    English X referencesErythroderma Ichthyosiforme, Bullous
    Ichthyosiform Erythroderma, Bullous Congenital
    Scope note in EnglishA form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode KERATIN-1 and KERATIN-10 have been associated with this disorder.
    See also reference (FX) in Slovak keratín-1
    keratín-10
    See also reference (FX) in English Keratin-1
    Keratin-10
    Links (3) - ARTICLES
    (2) - MeSH descriptor
    (1) - CiBaMed
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Number of the records: 1  

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