About Bilateral perisylvian polymicrogyria
Bilateral perisylvian polymicrogyria is a rare disease catalogued by Orphanet (ORPHA:98889). It is associated with the SRPX2, ADGRG1, PI4KA 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 Bilateral perisylvian polymicrogyria trials.
Search ClinicalTrials.gov for "Bilateral perisylvian polymicrogyria" or filter by Orphanet code ORPHA:98889 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 Bilateral perisylvian polymicrogyria trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Bilateral perisylvian polymicrogyria. Updated daily.