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伴有 TUBA4A 无义突变的单纯黑质病变尸检病例。

An autopsy case of pure nigropathy with TUBA4A nonsense mutation.

机构信息

University of Toyama School of Medicine, Toyama, Japan.

Department of Legal Medicine, Faculty of Medicine, University of Toyama, Toyama, Japan.

出版信息

Neuropathol Appl Neurobiol. 2021 Oct;47(6):891-893. doi: 10.1111/nan.12712. Epub 2021 Apr 5.

Abstract

We showed the results of pathological and genetic investigation for an autopsy case who was evaluated as longstanding Parkinson's disease (PD) in alive. Neuropathological investigation showed "pure nigropathy" without Lewy and tau pathology, and genetic analyses using next-generation sequencing detected novel TUBA4A nonsence mutation. Subsequent physiological study added to strength the hypothesis that the variant is pathogenic one. Present case showed TUBA4A is not only responsible gene for amyotrophic lateral sclerosis/frontotemporal dementia but also PD associated pure nigropathy. Also we found minimal but significant tau pathology high possibly associated with long-term deep brain stimulation in subthalamic nucleus.

摘要

我们展示了一例尸检病例的病理和遗传学研究结果,该病例生前被评估为长期帕金森病(PD)。神经病理学研究显示“纯黑质病变”,无路易体和 tau 病理学,使用下一代测序的基因分析检测到新型 TUBA4A 无义突变。随后的生理研究进一步支持了该变异具有致病性的假说。本病例表明 TUBA4A 不仅是肌萎缩侧索硬化症/额颞叶痴呆的致病基因,也是与 PD 相关的纯黑质病变的致病基因。此外,我们还发现了少量但显著的 tau 病理学,可能与长期丘脑底核深部脑刺激有关。

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