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[颅颈肌张力障碍。实用的一般概念还是疾病实体?]

[Craniocervical dystonia. Pragmatic general concept or nosologic entity?].

作者信息

Csala B, Deuschl G

机构信息

Neurologische Klinik und Poliklinik, Universität Freiburg.

出版信息

Nervenarzt. 1994 Feb;65(2):75-94.

PMID:8164772
Abstract

The focal dystonias of cranial-nerve innervated muscles are described. They include the ocular dystonia, blepharospasmus and other facial dystonias, mandibular dystonia, pharyngeal dystonia, spasmodic dysphonia, external laryngeal dystonia, spasmodic torticollis and lingual dystonia. They share similar clinical aspects such as the inadequate co-contraction of antagonistic muscles, dystonic overflow of muscle activity to muscles not normally involved, similar facilitating and inhibitory activities and various "antagonistic gestures". Genetic, imaging, neuroanatomic, physiologic and pharmacologic findings suggest common pathogenetic mechanisms for these diseases. Similar therapeutic approaches are established. The frequent and variable combinations of these focal dystonias and their similar pathogenetic background favour their common classification as craniocervial dystonias.

摘要

本文描述了由颅神经支配肌肉的局灶性肌张力障碍。它们包括眼睑痉挛、睑痉挛和其他面部肌张力障碍、下颌肌张力障碍、咽部肌张力障碍、痉挛性发声障碍、喉外肌张力障碍、痉挛性斜颈和舌肌张力障碍。它们具有相似的临床特征,如拮抗肌协同收缩不足、肌肉活动异常扩散至通常不参与的肌肉、相似的易化和抑制活动以及各种“拮抗姿势”。遗传学、影像学、神经解剖学、生理学和药理学研究结果表明这些疾病存在共同的发病机制。已确立了相似的治疗方法。这些局灶性肌张力障碍的频繁且多样的组合及其相似的发病背景有利于将它们共同归类为颅颈肌张力障碍。

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