What's New in Paroxysmal Movement Disorders

被引:0
|
作者
Zittel, S. [1 ]
Muenchau, A. [1 ]
机构
[1] Univ Klin Hamburg Eppendorf, Klin Neurol, D-20246 Hamburg, Germany
关键词
paroxysmal kinesigenic dyskinesia; paroxysmal non-kinesigenic dyskinesia; paroxysmal exercise-induced dyskinesia; FAMILIAL INFANTILE CONVULSIONS; NON-KINESIGENIC DYSKINESIA; EXERCISE-INDUCED DYSTONIA; PRRT2; MUTATIONS; CLINICAL-FEATURES; GLUT1; MAJOR CAUSE; CHOREOATHETOSIS; GENE; EPILEPSY;
D O I
10.1055/s-0032-1327320
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Paroxysmal movement disorders are rare neurological disorders. Since some of these disorders have an excellent response to medical treatment it is important to consider them in the differential diagnosis of paroxysmal disorders. Autosomal dominantly inherited paroxysmal dyskinesias, in particular paroxysmal kinesigenic dyskinesia, represent the most common type of paroxysmal movement disorder. This article gives an over-view of the clinical characteristics of paroxysmal dyskinesias and summarises new insights into the genetics and pathophysiology of these disorders. We describe the phenotypic variability of specific gene mutations to highlight the close link between paroxysmal dyskinesias and others paroxysmal disorders.
引用
收藏
页码:463 / 466
页数:4
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