Carbamazepine-Induced Juvenile Myoclonic Seizures

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Treatment of myoclonic seizures in patients with juvenile myoclonic epilepsy

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Oxcarbazepine-induced myoclonic status epilepticus in juvenile myoclonic epilepsy.

Juvenile myoclonic epilepsy (JME) is a frequent idiopathic generalised epilepsy syndrome with typical clinical and EEG features that can usually be controlled by valproate monotherapy. JME may be underdiagnosed or misdiagnosed; in the latter case, it may be mistaken for partial epilepsy. The incorrect diagnosis of JME is likely to result in inappropriate therapy, which may, in turn, worsen the ...

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ژورنال

عنوان ژورنال: Pediatric Neurology Briefs

سال: 2000

ISSN: 2166-6482,1043-3155

DOI: 10.15844/pedneurbriefs-14-11-10