Kyoto University Graduate School of Medicine and Takeda General Hospital, Kyoto, Japan.
Mov Disord. 2011 May;26(6):1142-8. doi: 10.1002/mds.23673.
This review examines some of the advances in understanding myoclonus over the last 25 years. The classification of myoclonus into cortical, brainstem, and spinal forms has been consolidated, each with distinctive clinical characteristics and physiological mechanisms. New genetic causes of myoclonus have been identified, and the molecular basis of several of these conditions has been discovered. It is increasingly apparent that disease of the cerebellum is particularly important in the genesis of cortical reflex myoclonus. However, the precise mechanism and origin of myoclonus in many situations remain uncertain. Effective treatment of myoclonus remains limited, and the challenge lies ahead to develop more therapeutic options.
这篇综述回顾了过去 25 年来人们对肌阵挛认识的一些进展。肌阵挛的分类已被巩固为皮质、脑干和脊髓形式,每种形式都具有独特的临床特征和生理机制。新的肌阵挛遗传病因已被确定,其中一些疾病的分子基础已被发现。越来越明显的是,小脑疾病在皮质反射性肌阵挛的发病机制中尤为重要。然而,在许多情况下,肌阵挛的确切机制和起源仍不确定。肌阵挛的有效治疗仍然有限,未来的挑战在于开发更多的治疗选择。