About Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder is a rare disease catalogued by Orphanet (ORPHA:500180). It is associated with the UBTF 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 motor and cognitive regression syndrome with extrapyramidal movement disorder trials.
Search ClinicalTrials.gov for "Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder" or filter by Orphanet code ORPHA:500180 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 motor and cognitive regression syndrome with extrapyramidal movement disorder trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder. Updated daily.