LGI1 and autosomal dominant epilepsy with auditory features: The human leucine rich, glioma inactivated 1 (LGI1; GeneID 9211; MIM# 604619) gene has been linked to two different clinical phenotypes: malignant progression of glioma and autosomal dominant lateral temporal epilepsy (ADLTE; MIM# 600512), a rare familial partial epilepsy syndrome.