such as myoclonic-astatic syndrome, Dravet syndrome, Lennox–Gastaut syndrome, worsening epilepsy and status epilepticus. Infantile spasm is classified as an epileptic encephalopathy with a poor ...

At the age of five months, the children presented with repeated vomiting and developed strabismus, progressive muscular hypotonia, myoclonic epilepsy and psychomotor regression. A cranial CT-scan ...

A recent report has described the use of video-electroencephalography (video-EEG) in the management of patients with atypical juvenile myoclonic epilepsy (JME). The work highlights the importance ...

It is currently being used in the treatment of multiple seizure disorders, including generalized tonic-clonic; absence; myoclonic, especially juvenile myoclonic; Lennox-Gastaut syndrome ...