Juvenile Myoclonic Epilepsy

Juvenile myoclonic epilepsy (JME) is an epileptic condition that develops in children and adolescents, invariably between the ages of 8 and 26 with most of the seizures occurring between the ages of 12 and 18. The frequency in the population is between 3% and 11%. JME is also called as Janz syndrome.
Email bookmark
Font : A-A+

Related Links