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Table 1 Demographic and clinical characteristics of patients with Lennox-Gastaut syndrome

From: Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome

 

LGS (N = 50)

Cryptogenic LGS (N = 28)

Symptomatic LGS (N = 22)

p

Gender (male/female)

38/12

21/7

17/5

0.852

Age at conclusion of study (years)

12.9 ± 6.5

12.5 ± 6.1

13.5 ± 7.1

0.875

Age at evaluation (years)

9.3 ± 6.2

9.9 ± 5.6

8.4 ± 7.0

0.418

Age at seizure onset (months)

35.3 ± 29.6

49.4 ± 29.5

17.4 ± 18.1

0.007*

Seizure type

 Tonic

48 (96%)

26 (92.9%)

22 (100.0%)

0.309

 GTCS/secondary GTCS

34 (68%)

18 (64.3%)

16 (72.7%)

0.525

 Complex/simple partial

20 (40%)

11 (39.3%)

9 (40.9%)

0.907

 Atypical absence

20 (40%)

12 (42.9%)

8 (36.4%)

0.642

 Myoclonic

16 (32%)

8 (28.6%)

8 (36.4%)

0.558

 Spasms

12 (24%)

1 (3.6%)

11 (50.0%)

0.001*

 Drops

11 (22%)

5 (17.9%)

6 (27.3%)

0.650

 Atonic

8 (16%)

5 (17.9%)

3 (13.6%)

0.988

Status epilepticus

6 (12%)

3 (10.7%)

3 (13.6%)

1.000

EEG characteristics

 Slow background activity

34 (68%)

18 (64.3%)

16 (72.7%)

0.525

 Generalized polyspikes

49 (98%)

28 (100.0%)

21 (95.5%)

0.440

 Diffuse SSW pattern

36 (72%)

22 (78.6%)

14 (63.6%)

0.243

 Focal discharges

43 (86%)

24 (85.7%)

19 (86.4%)

1.000

 Burst-suppression pattern

11 (22%)

6 (21.4%)

5 (22.7%)

1.000

Antiepileptic drugs

 2

13 (26%)

10 (35.7%)

3 (13.6%)

0.768

 ≥ 3

37 (74%)

18 (64.3%)

19 (86.4%)

 

Seizure free

14 (28%)

13 (46.4%)

1 (4.5%)

0.001*

  1. GTCS generalized tonic-clonic seizure, SSW slow spike-wave
  2. * p < 0.05 (two-sided) was statistically significant