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阵发性运动障碍。

Paroxysmal movement disorders.

机构信息

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.

出版信息

Handb Clin Neurol. 2024;203:145-156. doi: 10.1016/B978-0-323-90820-7.00010-0.

DOI:10.1016/B978-0-323-90820-7.00010-0
PMID:39174246
Abstract

Paroxysmal movement disorders include two groups of intermittent neurologic disorders: paroxysmal dyskinesia, in which episodes of involuntary hyperkinetic movements (mainly chorea and/or dystonia) occur with preserved consciousness, and episodic ataxias, which are characterized by discrete attacks of cerebellar dysfunction, sometimes associated with progressive ataxia. Since episodic ataxias are individually discussed in Chapter 8 of this volume, we herein provide a deep overview of phenotypic, genetic, pathophysiologic, diagnostic, and treatment aspects of paroxysmal dyskinesia, following the trigger-based nomenclature which distinguishes paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigenic dyskinesia, and paroxysmal exercise-induced dyskinesia. Emerging paroxysmal dyskinesia not fulfilling the criteria for the above-mentioned subtypes will also be discussed. Phenotypic and genotypic overlap among paroxysmal movement disorders, epilepsy, and migraine have progressively emerged, thus shedding light on a shared pathophysiologic framework. Advances in our understanding of the pathomechanisms underlying paroxysmal movement disorders, which involve dysfunctions of ion channels, proteins associated with the vesical synaptic cycle machinery, and proteins involved in neuronal energy metabolism, point toward a discrete number of converging pathophysiologic pathways and may lay foundations for developing target-specific therapies.

摘要

发作性运动障碍包括两组间歇性神经障碍

发作性运动障碍,其特征是无意识的运动障碍(主要为舞蹈症和/或肌张力障碍)发作,意识保持清醒;发作性共济失调,其特征是小脑功能障碍的离散发作,有时伴有进行性共济失调。由于发作性共济失调在本卷第 8 章中单独讨论,因此我们在此根据基于触发因素的命名法提供发作性运动障碍的表型、遗传、病理生理、诊断和治疗方面的深入概述,该命名法区分了发作性运动诱发性运动障碍、发作性非运动诱发性运动障碍和发作性运动障碍。还将讨论不符合上述亚型标准的新发发作性运动障碍。发作性运动障碍、癫痫和偏头痛之间的表型和基因型重叠逐渐显现,从而揭示了共同的病理生理框架。我们对发作性运动障碍的病理机制的理解的进展,涉及离子通道、与囊泡突触循环机制相关的蛋白以及参与神经元能量代谢的蛋白的功能障碍,指向少数几个趋同的病理生理途径,并可能为开发针对特定靶点的治疗方法奠定基础。

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