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. Author manuscript; available in PMC: 2021 Jul 1.
Published in final edited form as: Epilepsia. 2020 Jun 18;61(7):1427–1437. doi: 10.1111/epi.16569

Table 1:

Sample Characteristics

Epilepsy Controls
Subjects (n) 183 107
Age 12.2 (3.1) 12.4 (3.0)
Gender 90 male, 93 female 54 male, 53 female
Grade 6.5 (3.3) 6.6 (2.7)
Full Sacle IQ 101.4 (13.7) 109.3 (11.3)
No/Mono/Poly 29/144/10
Syndrome (IGE1/LRE2) 91/92

Notes:

1

IGE composed of the following syndromes: juvenile myoclonic epilepsy [JME](n=42), childhood and juvenile absence [Absence] (n=33), and IGE not otherwise specified [NOS] (n=16)).

2

LRE composed of the following syndromes: benign epilepsy with centrotemporal spikes [BECTS] (n=41), temporal lobe epilepsy [TLE] (n=20), frontal lobe epilepsy [FLE] (n=8), occipital lobe epilepsy (n=3) and focal epilepsy NOS (n=20)). For syndromic analyses the groups with temporal and frontal lobe syndrome were combined (FLE/TLE) (n=28) and occipital lobe epilepsy excluded.