Autosomal recessive palmoplantar keratoderma and congenital alopecia

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.

Also known as: PPK-CA, Wallis type, autosomal recessive palmoplantar hyperkeratosis and congenital alopecia, cataract-alopecia-sclerodactyly syndrome, palmoplantar keratoderma and congenital alopecia type 2, palmoplantar keratoderma and congenital alopecia, Wallis type, PPKCA2, Ppkca, Wallis type, cass

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