familial temporal lobe epilepsy 4
MeSH: C566902ORPHA: 98819
Overview
temporal lobe epilepsy characterized by autosomal dominant inheritance of occipitotemporal lobe epilepsy and migraine with visual aura and that has material basis in variation in the chromosome region 9q21-q22
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566902Orphanet Code
ORPHA:98819familial temporal lobe epilepsy 4
| MeSH | C566902 |
| Orphanet | ORPHA:98819 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO