Progressive myoclonic epilepsies

被引:8
|
作者
Conry, JA [1 ]
机构
[1] Childrens Natl Med Ctr, Washington, DC 20010 USA
关键词
D O I
10.1177/08830738020170011201
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The progressive myoclonic epilepsies area rare but extremely debilitating group or disorders that are difficult to generalized epilepsy. Efficacy and even harder to treat. They represent a heterogeneous subgroup of those with secondary generalized epilepsy. Efficacy of treatment is often Measured in terms of slowing a patient's inevitable decline. Reviewed here are the classification of progressive myoclonic epilepsies, features of myoclonic seizures, the five most prevalent progressive myoclonic epilepsy syndromes-Unverricht-Lundborg disease, myoclonus epilepsy with ragged red fibers (MERRF) mitochondrial disease, Lafora's disease, neuronal ceroid lipofuscinoses, and sialidoses-and current treatment options.
引用
收藏
页码:S80 / S84
页数:5
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