Autosomal recessive palmoplantar keratoderma and congenital alopecia

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Synonyms: Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia | Cataract-alopecia-sclerodactyly syndrome | PPK-CA, Wallis type | Palmoplantar keratoderma and congenital alopecia, Wallis type

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024

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