临床运动功能障碍的常见模式。

Muscle & nerve. Supplement Pub Date : 1997-01-01
N H Mayer, A Esquenazi, M K Childers
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引用次数: 0

摘要

上运动神经元综合征通常导致继发于激动性肌无力、拮抗性肌痉挛和痉挛肌肉流变学(僵硬)特性改变的典型畸形模式的发展。识别导致关节畸形的痉挛肌肉,使治疗性去神经支配的实施具有最大的成功可能性。识别负责的肌肉可能是复杂的,因为许多肌肉可能穿过所涉及的关节,并不是所有有可能导致畸形的肌肉都会痉挛。包括多肌电图和局部麻醉诊断阻滞在内的策略可用于测试有关畸形的假设,为更长期的去神经控制提供信息。在这篇综述中,我们讨论了常见的与问题性痉挛、瘫瘫、挛缩和自主运动控制受损相关的畸形模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Common patterns of clinical motor dysfunction.

An upper motor neuron syndrome often leads to the development of stereotypical patterns of deformity secondary to agonist muscle weakness, antagonist muscle spasticity and changes in the rheologic (stiffness) properties of spastic muscles. Identification of the spastic muscles that contribute to deformity across a joint allows therapeutic denervation to be implemented with the maximum likelihood of success. Identifying responsible muscles can be complex, since many muscles may cross the joint involved, and not all muscles with the potential to cause deformity will be spastic. Strategies including polyelectromyography and diagnostic blocks with local anesthetics can be used to test hypotheses regarding the deformity, providing information for more long-term denervation. In this review, we discuss frequently observed patterns of deformity associated with problematic spasticity, paresis, contracture, and impaired voluntary motor control.

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