/autosomal recessive palmoplantar keratoderma and congenital alopecia

autosomal recessive palmoplantar keratoderma and congenital alopecia

Rare Disease

MONDO:0008923

Also Known As

PPK-CA, Wallis typeautosomal recessive palmoplantar hyperkeratosis and congenital alopeciacataract-alopecia-sclerodactyly syndromepalmoplantar keratoderma and congenital alopecia type 2palmoplantar keratoderma and congenital alopecia, Wallis typePPKCA2Ppkca, Wallis typecasscataract, alopecia, sclerodactylycataract, alopecia, sclerodactyly syndromepalmoplantar keratoderma and congenital alopecia 2

Definition

Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by congenital alopecia and palmoplantar hyperkeratosis. It is usually associated with cataracts, progressive sclerodactyly and pseudo-ainhum.