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 October 2024
Newly diagnosed with
Autosomal dominant palmoplantar keratoderma and congenital alopecia?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
National Foundation for Ectodermal Dysplasias
The NFED mission is to empower and connect those touched by ectodermal dysplasias through education, support and research.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.