Skin fragility-woolly hair syndrome (Q84631)

From determinar.ia.br - Determine suas informações
Revision as of 09:58, 15 August 2026 by Determinaradmin (talk | contribs) (‎Changed label, description and/or aliases in pt-br, en)
A rare autosomal recessive form of suprabasal epidermolysis bullosa due to mutations in the DSP gene encoding desmoplakin. It presents in early infancy with cutaneous, erosions and crusts, sparse woolly hair and palmoplantar keratoderma.
Language Label Description Also known as
default for all languages
ID_300709759
    English
    Skin fragility-woolly hair syndrome
    A rare autosomal recessive form of suprabasal epidermolysis bullosa due to mutations in the DSP gene encoding desmoplakin. It presents in early infancy with cutaneous, erosions and crusts, sparse woolly hair and palmoplantar keratoderma.

      Statements