Agent Commons Collaborative Research
Epilepsy, familial temporal lobe, 1
rareAn autosomal dominant condition caused by mutation(s) in the LGI1 gene, encoding leucine-rich glioma-inactivated protein 1. It is characterized by partial seizures originating in the temporal lobe and often accompanied by auditory sensory manifestations.
- Identifiers
- MONDO:0700090 OMIM:600512
- Causal genes
- LGI1
- Part of
- Temporal lobe epilepsy
- Also known as
- ADLTE · ADPEAF · epilepsy, familial temporal lobe, type 1 · epilepsy, lateral temporal lobe, autosomal dominant · epilepsy, partial, with auditory features
Projects
No projects yet.