Juvenile Myoclonic Epilepsy
Also written as JME.
Juvenile absence seizures are similar to typical absences but occur at a later age and are accompanied by 4- to 6-Hz spike-and–slow-wave and polyspike and– slow-wave discharges.\nThese are usually associated with juvenile myoclonic epilepsy.
What our notes say
- Juvenile absence seizures are similar to typical absences but occur at a later age and are accompanied by 4- to 6-Hz spike-and–slow-wave and polyspike and– slow-wave discharges.\nThese are usually associated with juvenile myoclonic epilepsy. (Convulsive Disorders)
- Juvenile myoclonic epilepsy (Janz syndrome) is the most common generalized epilepsy in young adults, accounting for 5% of all epilepsies. (Convulsive Disorders)
- Rolandic epilepsy, Juvenile myoclonic epilepsy (JME) to\nUnprovoked seizures are the result of a brain disorder mention a few. (Devendra K. Gupta, Krishna M. Goel - Hutchison’s Paediatrics. chdhe-Jaypee Broth)
- Lamotrigine ● Dravet’s syndrome,\n● Juvenile myoclonic epilepsy\n\n ● Is there any other modality of treatments?\n○ Epilepsy surgery\n○ Vagal Nerve stimulation\n○ Ketogenic diet (26. Seizure)