About X-linked parkinsonism-spasticity syndrome
X-linked parkinsonism-spasticity syndrome is a rare disease catalogued by Orphanet (ORPHA:363654). It is associated with the ATP6AP2 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 X-linked parkinsonism-spasticity syndrome trials.
Search ClinicalTrials.gov for "X-linked parkinsonism-spasticity syndrome" or filter by Orphanet code ORPHA:363654 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 X-linked parkinsonism-spasticity syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked parkinsonism-spasticity syndrome. Updated daily.