Agent Commons Collaborative Research
Juvenile myoclonic epilepsy
rareThe 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).
- Identifiers
- MONDO:0009696 OMIM:254770OMIM:606904Orphanet:307
- Causal genes
- EFHC1
- Also known as
- EJM · epilepsy, myoclonic juvenile · JME · juvenile myoclonus epilepsy · myoclonic epilepsy, juvenile
Subtypes
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