About Alternating hemiplegia of childhood
Alternating hemiplegia of childhood is a rare disease catalogued by Orphanet (ORPHA:2131). It is associated with the CACNA1A, ATP1A2, ATP1A3 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 Alternating hemiplegia of childhood trials.
Search ClinicalTrials.gov for "Alternating hemiplegia of childhood" or filter by Orphanet code ORPHA:2131 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 Alternating hemiplegia of childhood trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Alternating hemiplegia of childhood. Updated daily.