“…1 Our group provides strong evidence about the existence of a common, often unrecognized clinical entity called benign TLE, which is characterized by seizure onset in adulthood, frequent familial history, rare simple partial seizures, and radiologic evidence of hippocampal sclerosis (Hs) in almost 40%, which was previously considered synonymous with drug-resistant epilepsy. 2,3 Moreover, using voxel-based morphometry and cortical thickness we have confirmed mesial temporal lobe, parietal lobe, and thalamic abnormalities that were remarkably comparable to what is observed in patients with refractory TLE regardless of the presence of Hs. 4,5 Of interest, our observations in benign TLE are consistent with the brain regions reported by Keller et al 1 This finding further enlarges the thalamocortical network being observed, even in patients with very mild epilepsy.…”