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steatocystoma multiplex

  1. Subject h.steatocystoma multiplex
    Subject h.Steatocystoma Multiplex
    Entry termssteatocystóm mnohopočetný
    cysty mazových žliaz, mnohopočetné
    Scope note in EnglishA disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.
    See also reference (FX) in Slovak keratín-17
    See also reference (FX) in English Keratin-17
    Links (1) - ARTICLES
    (1) - MeSH descriptor
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Number of the records: 1  

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