familial temporal lobe epilepsy 8
ORPHA: 101046
Overview
temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with familial temporal lobe epilepsy 8, sourced from HPO and Orphanet clinical annotations.
Focal-onset seizureAuditory hallucinationEEG with focal epileptiform dischargesAphasiaInterictal epileptiform activityFocal aware seizureVisual hallucinationFocal autonomic seizureAbnormal autonomic nervous system physiologyNocturnal seizuresAtypical behaviorDepressionBilateral tonic-clonic seizureMigraineGeneralized-onset seizureBilateral tonic-clonic seizure with focal onsetImpulsivity
Classification & Codes
Orphanet Code
ORPHA:101046familial temporal lobe epilepsy 8
| Orphanet | ORPHA:101046 |
| Treatments | 0 drug(s) |
| Symptoms on record | 17 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO