About Progressive myoclonic epilepsy with dystonia
Progressive myoclonic epilepsy with dystonia is a rare disease catalogued by Orphanet (ORPHA:352596). It is associated with the TBC1D24 gene. 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 Progressive myoclonic epilepsy with dystonia trials.
Search ClinicalTrials.gov for "Progressive myoclonic epilepsy with dystonia" or filter by Orphanet code ORPHA:352596 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 Progressive myoclonic epilepsy with dystonia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Progressive myoclonic epilepsy with dystonia. Updated daily.