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. 2015 May 13;6:103. doi: 10.3389/fneur.2015.00103

Table 1.

Patient demographic data.

Controls RTLE LTLE
N 12 14 12
Age, y (SD) 29.4 (5.0) 36.2 (11.6) 35.9 (10.9)
Education, y (SD) 17.9 (4.3) 13.9 (3.8) 14.8 (2.8)
Sex, M/F 8/4 7/7 4/8
Handedness, R/L 11/1 12/2 11/1
Language dominance, R/L/BI 0/12/0 1/12/1 0/11/1
Disease duration, y (SD) 16.2 (14.2) 17.0 (11.8)
Onset of seizures, y (SD) 20.9 (13.5) 19.0 (16.0)
Presence of MTS, Yes/No 8/6 8/4
Other lesions 3 2
Verbal memory factor 0.11 (0.99) −0.20 (1.3)
Visual memory factor −0.24 (1.1) 0.59 (0.93)
IQ factor 0.11 (1.0) 0.38 (1.0)

RTLE, right temporal lobe epilepsy; LTLE, left temporal lobe epilepsy; y, years; SD, standard deviation; M, male; F, female; R, right; L, left; BI, bilateral; IQ, intelligence quotient.

Characterization of MTS and other lesions was based on radiology (3 T MRI protocol). Three patients with RTLE showed right MTL cortical dysplasia, one with dual pathology of MTS. With respect to extra-MTL lesions, MRI demonstrated cortical dysplasia in the left posterior insula surrounding Heschl’s gyrus in one LTLE patient (with concomitant MTS) and a heterotopion in the left occipital horn in another LTLE patient. All patients were subsequently referred for standard anterior temporal lobe resections.