About OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature
OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature is a rare disease catalogued by Orphanet (ORPHA:306762). 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 worldwide.
Clinical Trial Eligibility Tips
What to know before applying to OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature trials.
Search ClinicalTrials.gov for "OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature" or Orphanet code ORPHA:306762 to find disease-specific recruiting studies.
Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.
Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.
Patient Resources
Find recruiting OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature. Updated daily.