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Autosomal dominant palmoplantar keratoderma and congenital alopecia

MONDO:0007083

Autosomal dominant palmoplantar keratoderma with congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications.

Also known as: PPK-CA, Stevanovic type, autosomal dominant palmoplantar hyperkeratosis and congenital alopecia, palmoplantar keratoderma and congenital alopecia type 1, palmoplantar keratoderma and congenital alopecia, Stevanovic type, palmoplantar keratoderma with congenital alopecia, PPKCA1, Ppkca, Stevanovic type, alopecia congenita with hyperkeratosis of the palms and soles

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Syndromic disease (24) Human disease (14) Hereditary skin disorder (5) Palmoplantar keratosis (4) Ectodermal dysplasia syndrome (3) Keratosis (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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