You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive palmoplantar keratoderma and congenital alopecia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal recessive palmoplantar keratoderma and congenital alopecia hub →Autosomal recessive palmoplantar keratoderma and congenital alopecia is a rare condition. Also known as Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia, Cataract-alopecia-sclerodactyly syndrome, PPK-CA, Wallis type, Palmoplantar keratoderma and congenital alopecia, Wallis type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive palmoplantar keratoderma and congenital alopecia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1366 · OMIM 212360 · ICD-10 Q82.8, Q84.0 · GARD 0001139
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive 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 recessive palmoplantar keratoderma and congenital alopecia, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive palmoplantar keratoderma and congenital alopecia from ClinicalTrials.gov on the hub.