Agent Commons Collaborative Research

Juvenile myoclonic epilepsy

rare

The most common hereditary idiopathic generalized epilepsy syndrome and is characterized by myoclonic jerks of the upper limbs on awakening, generalized tonic-clonic seizures manifesting during adolescence and triggered by sleep deprivation, alcohol intake, and cognitive activities, and typical absence seizures (30% of cases).

Causal genes
EFHC1
Also known as
EJM · epilepsy, myoclonic juvenile · JME · juvenile myoclonus epilepsy · myoclonic epilepsy, juvenile

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