myoclonic epilepsy
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Clinical manifestations
Management
- patients with juvenile myoclonic epilepsy require lifelong anticonvulsant therapy[1]
More general terms
More specific terms
- juvenile myoclonic epilepsy (of Janz)
- Lennox-Gastaut syndrome (epileptic encephalopathy, Lennox-Gastaut type)
- myoclonus epilepsy of Unverricht-Lundborg (EPM1)
- progressive myoclonic epilepsy 2A; myoclonic epilepsy of Lafora (MELF)
- progressive myoclonic epilepsy type 1
- severe myoclonic epilepsy in infancy (SMEI); Dravet syndrome