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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.

Juvenile Myoclonic Epilepsy - It is a form of generalized seizure characterized by sudden jerky movements of both arms and shoulders - They usually occur after waking up in the mornings

Juvenile Myoclonic Epilepsy

Juvenile myoclonic epilepsy is a form of generalized seizure characterized by sudden jerky movements of both arms and shoulders, usually just after waking up. Read More

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