You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant palmoplantar keratoderma and congenital alopecia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant palmoplantar keratoderma and congenital alopecia hub →Autosomal dominant palmoplantar keratoderma and congenital alopecia is a rare condition. Also known as Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia, PPK-CA, Stevanovic type, Palmoplantar keratoderma and congenital alopecia, Stevanovic type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant palmoplantar keratoderma and congenital alopecia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1010 · OMIM 104100 · ICD-10 Q82.8 · GARD 0000604
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant palmoplantar keratoderma and congenital alopecia, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Autosomal dominant palmoplantar keratoderma and congenital alopecia, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant palmoplantar keratoderma and congenital alopecia from ClinicalTrials.gov on the hub.