Neurological disorders caused by inherited ion-channel mutations

被引:47
作者
Kullmann, DM
Hanna, MG
机构
[1] UCL, Neurol Inst, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/S1474-4422(02)00071-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several neurological diseases-including neuromuscular disorders, movement disorders, migraine, and epilepsy-are caused by inherited mutations of ion channels. The list of these "channelopathies" is expanding rapidly, as is the phenotypic range associated with each channel. At present the best understood channelopathies are those that affect muscle-fibre excitability. These channelopathies produce a range of disorders which include: periodic paralysis, myotonias, malignant hyperthermia, and congenital myasthenic syndromes. By contrast, the mechanisms of diseases caused by mutations of ion channels that are expressed in neurons are less well understood. However, as for the muscle channelopathies, a striking feature is that many neuronal channelopathies cause paroxysmal symptoms. This review summarises the clinical features of the known neurological channelopathies, within the context of the functions of the individual ion channels.
引用
收藏
页码:157 / 166
页数:10
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