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Results 1 - 4 of 4 for epidermolytic hyperkeratosis OR ichthyosis OR "keratoderma," palmoplantar
  1. KRT16 gene 
    ... K16 K1C16_HUMAN K1CP keratin 16 (focal non-epidermolytic palmoplantar keratoderma) keratin 16, type I keratin, type I cytoskeletal ...
    https://medlineplus.gov/genetics/gene/krt16 - Genetics
  2. Pachyonychia congenita 
    Pachyonychia congenita is a condition that primarily affects the skin and nails. The signs and symptoms of this condition usually become apparent within the first ...
    https://medlineplus.gov/genetics/condition/pachyonychia-congenita - Genetics
  3. KRT1 gene 
    ... body is usually not affected. A condition called epidermolytic palmoplantar keratoderma caused by KRT1 gene mutations is relatively mild. ... of KRT1 PubMed KERATIN 1, TYPE II; KRT1 PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, 1; EPPK1 ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE; IHCM ...
    https://medlineplus.gov/genetics/gene/krt1 - Genetics
  4. Epidermolytic hyperkeratosis 
    ... categorized into two types. People with PS-type epidermolytic hyperkeratosis have thick skin on the palms of their hands and soles of their feet (palmoplantar or palm/sole hyperkeratosis) in addition to other ...
    https://medlineplus.gov/.../condition/epidermolytic-hyperkeratosis - Genetics