About Epilepsy of infancy with migrating focal seizures
Epilepsy of infancy with migrating focal seizures is a rare disease catalogued by Orphanet (ORPHA:293181). It is associated with the SCN2A, KCNQ2, PIGA 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 Epilepsy of infancy with migrating focal seizures trials.
Search ClinicalTrials.gov for "Epilepsy of infancy with migrating focal seizures" or filter by Orphanet code ORPHA:293181 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 Epilepsy of infancy with migrating focal seizures trials
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