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特发性运动障碍的现象学和分类:共识更新。

Phenomenology and classification of dystonia: a consensus update.

机构信息

Department of Neurology, Catholic University, Milan, Italy.

出版信息

Mov Disord. 2013 Jun 15;28(7):863-73. doi: 10.1002/mds.25475. Epub 2013 May 6.

Abstract

This report describes the consensus outcome of an international panel consisting of investigators with years of experience in this field that reviewed the definition and classification of dystonia. Agreement was obtained based on a consensus development methodology during 3 in-person meetings and manuscript review by mail. Dystonia is defined as a movement disorder characterized by sustained or intermittent muscle contractions causing abnormal, often repetitive, movements, postures, or both. Dystonic movements are typically patterned and twisting, and may be tremulous. Dystonia is often initiated or worsened by voluntary action and associated with overflow muscle activation. Dystonia is classified along 2 axes: clinical characteristics, including age at onset, body distribution, temporal pattern and associated features (additional movement disorders or neurological features); and etiology, which includes nervous system pathology and inheritance. The clinical characteristics fall into several specific dystonia syndromes that help to guide diagnosis and treatment. We provide here a new general definition of dystonia and propose a new classification. We encourage clinicians and researchers to use these innovative definition and classification and test them in the clinical setting on a variety of patients with dystonia. © 2013 Movement Disorder Society.

摘要

本报告描述了一个由在该领域拥有多年经验的研究人员组成的国际小组的共识结果,他们审查了肌张力障碍的定义和分类。根据 3 次面对面会议期间的共识发展方法和邮件中的手稿审查,达成了一致意见。肌张力障碍定义为一种运动障碍,其特征为持续或间歇性肌肉收缩导致异常、通常是重复的运动、姿势或两者兼而有之。扭曲性运动通常是有模式的和扭曲的,可能是震颤性的。肌张力障碍通常由自愿运动引发或加重,并伴有肌肉过度激活。肌张力障碍沿着 2 个轴进行分类:临床特征,包括发病年龄、身体分布、时间模式和相关特征(其他运动障碍或神经特征);和病因,包括神经系统病理学和遗传。临床特征分为几种特定的肌张力障碍综合征,有助于指导诊断和治疗。我们在这里提供肌张力障碍的新的一般定义,并提出新的分类。我们鼓励临床医生和研究人员使用这些创新的定义和分类,并在各种肌张力障碍患者的临床环境中对其进行测试。© 2013 运动障碍学会。

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