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
Additional terms
References
- ↑ Jump up to: 1.0 1.1 Medical Knowledge Self Assessment Program (MKSAP) 11, American College of Physicians, Philadelphia 1998
Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022