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Medline ® Abstract for Reference 4

of 'Juvenile myoclonic epilepsy'

4
TI
Juvenile myoclonic epilepsy: clinical and EEG features.
AU
Pedersen SB, Petersen KA
SO
Acta Neurol Scand. 1998 Mar;97(3):160-3.
 
We aimed to characterize the clinical profile and EEG features of 43 patients with juvenile myoclonic epilepsy. In a retrospective design we studied the records of, and re-interviewed, 43 patients diagnosed with JME from the epilepsy clinic data base. Furthermore, available EEGs were re-evaluated. Of the patients 72% were female and 28% male. Average age of onset was 13 (5.5-22) years for absences, 16 (5.2-25) years for myoclonic seizures, and 16 (8-29) years for generalized tonic-clonic seizures. Forty-two percent reported asymmetric or unilateral myoclonic jerks. Commonly reported precipitating factors were sleep deprivation (84%), stress (70%), and alcohol consumption (51%). EEG findings included rapid spike-wave and polyspike-wave.
AD
Department of Orthopedic Surgery, Hvidovre Hospital, Denmark.
PMID