She was born to unrelated parents, had febrile seizures in infancy, but developed normally ... enhanced by photic stimulation. Juvenile myoclonic epilepsy was diagnosed and treatment with valproic ...

These include Dravet syndrome, myoclonic-astatic epilepsy, malignant migrating partial seizures in infancy, and LGS. Other conditions in which continuous abnormal EEG patterns are observed in ...

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 ...

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 ...