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.
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familial temporal lobe epilepsy 2
MONDO:0011965
familial temporal lobe epilepsy 4
MONDO:0012706
familial temporal lobe epilepsy 5
MONDO:0013741
familial temporal lobe epilepsy 6
MONDO:0014308
familial temporal lobe epilepsy 7
MONDO:0014639
familial temporal lobe epilepsy 8
MONDO:0014650