CENIR, Institut du Cerveau et de la Moelle Epiniere, Paris, France.
J Neurol. 2011 Nov;258(11):1911-9. doi: 10.1007/s00415-011-6107-9. Epub 2011 Jun 3.
Mirror movements (MM) are involuntary movements of one side of the body that accompany and mirror intentional movements on the opposite side. Physiological MM can occur during normal childhood development, probably owing to corpus callosum immaturity. Pathological congenital MM may be clinically isolated or part of a complex congenital syndrome, including Kallmann syndrome, Klippel-Feil syndrome, and congenital hemiplegia. Congenital isolated MM are usually familial. Recently, heterozygous mutations of the DCC gene, with autosomal dominant inheritance, were shown to cause some cases of MM. The pathogenesis of congenital MM may involve (i) abnormal interhemispheric inhibition between the two motor cortices; (ii) functional alteration of motor planning and motor execution; and/or (iii) abnormal persistence of the ipsilateral corticospinal tract. Fundamental and clinical research is providing novel insights into the complex underlying molecular pathways, and recent experimental work has identified several mechanisms that may mediate the motor network dysfunction. In this review, we analyze clinical, genetic, neurophysiologic, and neuroimaging data on congenital MM, and discuss how this knowledge may improve our understanding of bimanual motor control.
镜像运动(MM)是身体一侧的无意识运动,伴随着对侧的有意运动。生理 MM 可能在正常儿童发育过程中发生,可能归因于胼胝体不成熟。病理性先天性 MM 可能是临床孤立的,也可能是复杂先天性综合征的一部分,包括 Kallmann 综合征、Klippel-Feil 综合征和先天性偏瘫。先天性孤立性 MM 通常为家族性。最近,DCC 基因的杂合突变,具有常染色体显性遗传,被证明可引起一些 MM 病例。先天性 MM 的发病机制可能涉及(i)两个运动皮质之间异常的大脑半球间抑制;(ii)运动规划和运动执行的功能改变;和/或(iii)同侧皮质脊髓束的异常持续存在。基础和临床研究为复杂的潜在分子途径提供了新的见解,最近的实验工作确定了几种可能介导运动网络功能障碍的机制。在这篇综述中,我们分析了先天性 MM 的临床、遗传、神经生理和神经影像学数据,并讨论了这些知识如何有助于我们理解双手运动控制。