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LINGO1 变异与特发性震颤和帕金森病。

LINGO1 variants in essential tremor and Parkinson's disease.

机构信息

Center for Experimental Medicine, Department of Neurology, the Third Xiangya Hospital, Central South University, Changsha, HN, China.

出版信息

Acta Neurol Scand. 2012 Jan;125(1):1-7. doi: 10.1111/j.1600-0404.2011.01516.x. Epub 2011 Apr 7.

Abstract

The leucine-rich repeat and Ig domain containing 1 gene (LINGO1), recently considered to be conferred increased risk of essential tremor (ET), has been also implicated in Parkinson disease (PD). As the two common movement disorders have overlapping clinical and pathological features, it has been postulated that the LINGO1 gene may play a role in the pathogenesis of the two diseases. Here, we review published reports of the LINGO1 variants in ET and PD in an attempt to better understand the molecular and pathogenic relationship of LINGO1 to the two disorders.

摘要

富含亮氨酸重复和免疫球蛋白结构域的 1 号基因(LINGO1)最近被认为会增加特发性震颤(ET)的风险,也与帕金森病(PD)有关。由于这两种常见的运动障碍具有重叠的临床和病理特征,因此有人假设 LINGO1 基因可能在这两种疾病的发病机制中发挥作用。在这里,我们回顾了发表的关于 ET 和 PD 中 LINGO1 变体的报告,试图更好地了解 LINGO1 与这两种疾病的分子和发病机制关系。

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