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. 2017 Aug 24;8:63–65. doi: 10.1016/j.ebcr.2017.08.001

Table 2.

Individual description of cases.

Patient/sex Age/age at onset (years) GGE syndrome Persistent seizuresa Seizure frequency before LCMa ASD regime (mg/24 h) Clinical responseb Details
1/F 43/20 JME GTCS 1/6 m LCM 200
LEV 1000
Yes 2 y SzF on LCM up to date
2/M 39/6 CAE persisting into adulthood ABS and GTCS 2 GTCS/6 m
Weekly ABS
LCM 300
VPA 1200
LEV 1000
Yes After 3,5 y SzF on LCM, he suffered 2 GTCS (one provoked) in the last year
3/F 53/5 CAE persisting into adulthood GTCS 3/6 m LCM 400
LEV 3000
VPA 1000
Yes 6 y SzF on LCM up to date
4/M 48/14 GTCS alone GTCS 2/6 m LCM 200
VPA 1000
Yes ABS status on CBZ in the past
5 y SzF on LCM up to date
5/F 50/12 GTCS alone GTCS 3/6 m LCM 200
LEV 2000
Yes 3,5 y SzF on LCM up to date
6/M 63/10 JME ABS, myoclonic and GTCS 6 GTCS/6 m
NQ for myoclonic and ABS
LCM 300
VPA 1300
Yes 3 y SzF on LCM up to date
7/F 33/24 JAE ABS and GTCS 2 GTCS/6 m
NQ for ABS
(“sporadic”)
LCM 400
VPA 1600
Yes Subjective ABS increase
1,5 y GTCS-SzF on LCM up to date
8/M 35/17 GTCS alone GTCS 2/6 m LCM 400
VPA1500
No Similar. SzF after adding VPA to LCM (attributed to VPA)
9/M 58/11 JAE GTCS 2/6 m LCM 150
LTG 400
No Myoclonic and absence status

GTCS generalized tonic–clonic seizure; ABS absences; NQ not able to quantify; y years; m months; SzF seizure free; LEV levetiracetam; VPA valproate; LTG lamotrigine.

a

In the 6 months prior to LCM treatment onset.

b

50% or greater reduction in GTCS frequency.