Epilepsy, familial temporal lobe, 1

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.

Also known as: ADLTE, ADPEAF, ETL1, epilepsy, familial temporal lobe, type 1, epilepsy, lateral temporal lobe, autosomal dominant, epilepsy, partial, with auditory features

10 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial temporal lobe, 1 itself.