Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Temporal lobe epilepsy
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.
This condition has no sub-types.