About Paroxysmal kinesigenic dyskinesia
Paroxysmal kinesigenic dyskinesia is a rare disease catalogued by Orphanet (ORPHA:98809). It is associated with the PRRT2, KCNA1, KCNJ10 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 Paroxysmal kinesigenic dyskinesia trials.
Search ClinicalTrials.gov for "Paroxysmal kinesigenic dyskinesia" or filter by Orphanet code ORPHA:98809 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 Paroxysmal kinesigenic dyskinesia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Paroxysmal kinesigenic dyskinesia. Updated daily.