Juvenile myoclonic epilepsy
What is Juvenile myoclonic epilepsy?
An epilepsy syndrome typically beginning in early adolescence, and characterized by early morning myoclonic jerks that may progress into a generalized tonic-clonic seizure. A genetic disorder: some families have had gene linkage to chromosome-6. The EEG is characterized by generalized polyspike and wave discharges at 4–6 Hz.
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