Autosomal dominant palmoplantar keratoderma and congenital alopecia
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 April 2024
Newly diagnosed with
Autosomal dominant palmoplantar keratoderma and congenital alopecia?
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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.
Clinical Trials
For a list of clinical trials in this disease area, please click here.