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erythrokeratodermia variabilis

  1. Subject h.erythrokeratodermia variabilis
    Subject h.Erythrokeratodermia Variabilis
    Entry termserythro et keratodermia variabilis
    erythrokeratodermia figurata variabilis
    Greitherova choroba
    Mendes de Costov syndróm
    transgrediens et progrediens palmoplantar keratoderma
    erythro et keratodermia variabilis
    English X referencesErythrokeratodermia Figurata Variabilis
    Greither Disease
    Mendes De Costa Syndrome
    Scope note in EnglishAn autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA.
    See also reference (FX) in Slovak konexíny
    keratodermia palmoplantárna
    See also reference (FX) in English Connexins
    Keratoderma, Palmoplantar
    Links (2) - MeSH descriptor
    subject heading

    subject heading

Number of the records: 1  

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