You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary hyperekplexia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary hyperekplexia hub →Hereditary hyperekplexia is a rare condition. Also known as Congenital stiff man syndrome, Familial startle disease, Hereditary hyperexplexia, Kok disease, Stiff baby syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary hyperekplexia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3197 · OMIM 149400, 614618, 614619 · ICD-10 G25.8 · GARD 0003129
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary hyperekplexia, 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 Hereditary hyperekplexia, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary hyperekplexia from ClinicalTrials.gov on the hub.