Autosomal dominant palmoplantar keratoderma and congenital alopecia

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Name:
Autosomal dominant palmoplantar keratoderma and congenital alopecia
Description:
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications.
ORPHAcode:
1010
Synonyms:
Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia
PPK-CA, Stevanovic type
Palmoplantar keratoderma and congenital alopecia, Stevanovic type
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14