About Familial adult myoclonic epilepsy
Familial adult myoclonic epilepsy is a rare disease catalogued by Orphanet (ORPHA:86814). It is associated with the SAMD12, TNRC6A, RAPGEF2 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Familial adult myoclonic epilepsy trials.
Search ClinicalTrials.gov for "Familial adult myoclonic epilepsy" or filter by Orphanet code ORPHA:86814 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Familial adult myoclonic epilepsy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial adult myoclonic epilepsy. Updated daily.