You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Dejerine-Sottas disease, look for clinical trials, and connect with others living with it — all in one place.
Open the full Dejerine-Sottas disease hub →Dejerine-Sottas disease is a rare condition. Also known as Charcot-Marie-Tooth disease type 3, HMSN 3, HMSN III, Hereditary motor and sensory neuropathy type 3, Hereditary motor and sensory neuropathy type III. Tomeko brings together the specialists, research, clinical trials, treatments and community for Dejerine-Sottas disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:64748 · OMIM 145900, 618184 · ICD-10 G60.0 · GARD 0009204
Start by learning the basics from an authoritative source, find a specialist or center that sees Dejerine-Sottas disease, 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 Dejerine-Sottas disease, filtered to your area.
Tomeko shows live, recruiting studies for Dejerine-Sottas disease from ClinicalTrials.gov on the hub.