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LRRK2 基因突变致帕金森病的神经病理学研究

Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2.

机构信息

Department of Neurology, Hospital Donostia, Paseo Dr. Beguiristain s.n, 20014 Donostia, San Sebastián, Gipuzkoa, Spain.

出版信息

Mov Disord. 2009 Oct 15;24(13):1998-2001. doi: 10.1002/mds.22677.

Abstract

We report the neuropathological findings in a patient with Parkinson's disease (PD) associated with Basque R1441G-LRRK2/dardarin mutation. The patient was a man with disease onset at 68 years of age, with unilateral rest tremor; the Parkinsonism was well controlled with medication for 15 years. He died at the age of 86, after 18 years of evolution. The neuropathological examination disclosed mild neuronal loss in the substantia nigra pars compacta without alpha-synuclein, tau, LRRK2, or ubiquitin cytoplasmic inclusions. Lewy bodies and Lewy neurites were absent. This is the first neuropathological study of PD associated with brain with the R1441G mutation in LRRK2.

摘要

我们报告了一例帕金森病(PD)伴巴斯克 R1441G-LRRK2/dardarin 突变患者的神经病理学发现。患者为男性,68 岁发病,表现为单侧静止性震颤;帕金森病经药物治疗 15 年得到很好的控制。18 年后,他在 86 岁时去世。神经病理学检查显示黑质致密部神经元轻度丢失,无α-突触核蛋白、tau、LRRK2 或泛素细胞质包涵体。路易体和路易神经突缺失。这是首例与 LRRK2 中 R1441G 突变相关的帕金森病伴脑的神经病理学研究。

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