About Familial mesial temporal lobe epilepsy with febrile seizures
Familial mesial temporal lobe epilepsy with febrile seizures is a rare disease catalogued by Orphanet (ORPHA:165805). 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 worldwide.
Clinical Trial Eligibility Tips
What to know before applying to Familial mesial temporal lobe epilepsy with febrile seizures trials.
Search ClinicalTrials.gov for "Familial mesial temporal lobe epilepsy with febrile seizures" or Orphanet code ORPHA:165805 to find disease-specific recruiting studies.
Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.
Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.
Patient Resources
Find recruiting Familial mesial temporal lobe epilepsy with febrile seizures trials
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