About Genetic epilepsy with febrile seizure plus
Genetic epilepsy with febrile seizure plus is a rare disease catalogued by Orphanet (ORPHA:36387). It is associated with the HCN1, SLC32A1, FGF13 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 Genetic epilepsy with febrile seizure plus trials.
Search ClinicalTrials.gov for "Genetic epilepsy with febrile seizure plus" or filter by Orphanet code ORPHA:36387 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 Genetic epilepsy with febrile seizure plus trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Genetic epilepsy with febrile seizure plus. Updated daily.