Conditions / Genetic
familial temporal lobe epilepsy 1
info ยท Genetic
A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome
A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome 10q24.
Signs and symptoms
- Bilateral tonic-clonic seizure
- Bilateral tonic-clonic seizure with focal onset
- Focal aware seizure
- Focal sensory seizure with auditory features
- Focal autonomic seizure with epigastric sensation/nausea/vomiting/other gastrointestinal phenomena
- Focal impaired awareness seizure
- Focal aware sensory seizure with auditory features
- Focal sensory seizure with cephalic sensation
- Focal sensory seizure with visual features
- Focal sensory seizure with vestibular features
Also known as: ETL1; partial epilepsy with auditory features