A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22.
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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 8
MONDO:0014650
epilepsy, familial temporal lobe, 1
MONDO:0700090