Disease Directory Self-limited infantile epilepsy
Neurological

Self-limited infantile epilepsy

Type

Disease

Gene

SCN8A, SCN2A, KCNQ2, KCNQ3, PRRT2

About Self-limited infantile epilepsy

Self-limited infantile epilepsy is a rare disease catalogued by Orphanet (ORPHA:306). It is associated with the SCN8A, SCN2A, KCNQ2 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 Self-limited infantile epilepsy trials.

Search ClinicalTrials.gov for "Self-limited infantile epilepsy" or filter by Orphanet code ORPHA:306 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

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:306)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Self-limited infantile epilepsy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Self-limited infantile epilepsy. Updated daily.