You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Benign adult familial myoclonic epilepsy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Benign adult familial myoclonic epilepsy hub →Benign adult familial myoclonic epilepsy is a rare condition. Also known as ADCME, Autosomal dominant cortical myoclonus and epilepsy, BAFME, Benign adult familial myoclonus epilepsy, FAME, FCMTE, Familial cortical myoclonic tremor and epilepsy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Benign adult familial myoclonic epilepsy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:86814 · OMIM 601068, 607876, 613608 · ICD-10 G40.3 · GARD 0016758
Start by learning the basics from an authoritative source, find a specialist or center that sees Benign adult familial myoclonic epilepsy, 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 Benign adult familial myoclonic epilepsy, filtered to your area.
Tomeko shows live, recruiting studies for Benign adult familial myoclonic epilepsy from ClinicalTrials.gov on the hub.