Familial temporal lobe epilepsy 2
MONDO:0011965A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has material basis in variation in the chromosome region 12q22-q23.3.
Also known as: ETL2, familial temporal lobe epilepsy type 2, Ftle, epilepsy, familial temporal lobe, epilepsy, familial temporal lobe, 2, familial temporal lobe epilepsy, temporal epilepsy, familial
10 clinical trials for this condition and its sub-types, 0 tagged with Familial temporal lobe epilepsy 2 itself.
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