About Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity is a rare disease catalogued by Orphanet (ORPHA:53583). It is associated with the SLC2A1 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 Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity trials.
Search ClinicalTrials.gov for "Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity" or filter by Orphanet code ORPHA:53583 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 dystonic choreathetosis with episodic ataxia and spasticity trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity. Updated daily.