About Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression is a rare disease catalogued by Orphanet (ORPHA:391316). It is associated with the TNK2 gene. 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 Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression trials.
Search ClinicalTrials.gov for "Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression" or filter by Orphanet code ORPHA:391316 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 Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression. Updated daily.