You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome hub →Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome is a rare condition. Also known as Palmoplantar keratoderma-Charcot-Marie-Tooth syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:538574 · OMIM 148360 · ICD-10 G60.0 · GARD 0017977
Start by learning the basics from an authoritative source, find a specialist or center that sees Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome, 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 Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome from ClinicalTrials.gov on the hub.