Synonyms: Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia | PPK-CA, Stevanovic type | Palmoplantar keratoderma and congenital alopecia, Stevanovic type
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma without other hand complications.
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 2026
Newly diagnosed with
Autosomal dominant palmoplantar keratoderma and congenital alopecia?
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Advocacy Organizations
National Foundation for Ectodermal Dysplasias
Together, we enrich the lives of people affected by ectodermal dysplasias by fostering community, providing education and support, and driving advocacy and groundbreaking research—creating a brighter future for all.
Uganda Alliance of Patients Organization
Supporting patients to access quality, safe and patient-centered healthcare services.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.