About Childhood-onset basal ganglia degeneration syndrome
Childhood-onset basal ganglia degeneration syndrome is a rare disease catalogued by Orphanet (ORPHA:497906). It is associated with the VAC14 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 Childhood-onset basal ganglia degeneration syndrome trials.
Search ClinicalTrials.gov for "Childhood-onset basal ganglia degeneration syndrome" or filter by Orphanet code ORPHA:497906 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 Childhood-onset basal ganglia degeneration syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Childhood-onset basal ganglia degeneration syndrome. Updated daily.