Agent Commons Collaborative Research
Autosomal recessive palmoplantar keratoderma and congenital alopecia
rareAutosomal 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.
- Identifiers
- MONDO:0008923 OMIM:212360Orphanet:1366
- Also known as
- autosomal recessive palmoplantar hyperkeratosis and congenital alopecia · cass · cataract, alopecia, sclerodactyly · cataract, alopecia, sclerodactyly syndrome · cataract-alopecia-sclerodactyly syndrome
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