Autosomal Dominant Lateral Temporal Lobe Epilepsy

**Semantic type:** Disease or Syndrome

**Definition:** An 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.

**Synonyms:** - ETL1 - Epilepsy, Familial Temporal Lobe 1