Etiological and pathogenetic mechanisms of forming muscle dystonias

S. E. Munasipova, Z. Zalyalova, A. A. Terekhova
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引用次数: 0

Abstract

This article discusses the issues of muscular dystonia pathogenesis that are relevant to modern medicine, as well as the possibility of using the pathogenetic concept as a substrate to supplement the classification criteria. Reviewing the international publications on etiopathophysiology, genetics and classification, the article summarizes the main mechanisms for the occurrence of a pathological process at different levels of the nervous system. Despite the frequent clinical similarity of the symptoms of various forms of muscular dystonia, these symptoms may be the result of dysfunction of completely different genetic and neurophysiological mechanisms. The article focuses on the importance of studying the etiological and pathogenetic mechanisms and their further implementation in clinical practice in order to develop more accurate treatment techniques aimed at eliminating the specific causes of the development of specific forms of muscular dystonia.
肌张力障碍形成的病因和发病机制
本文讨论了与现代医学相关的肌张力障碍发病机制问题,以及以发病概念为基础补充分类标准的可能性。本文综述了国际上在病因生理学、遗传学和分类方面的文献,总结了神经系统不同层次病理过程发生的主要机制。尽管各种形式的肌张力障碍的临床症状经常相似,但这些症状可能是完全不同的遗传和神经生理机制的功能障碍的结果。本文重点介绍了研究病因和发病机制及其在临床实践中的进一步应用的重要性,以便开发更准确的治疗技术,旨在消除特定形式肌张力障碍发展的特定原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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