Suppr超能文献

一个患有额颞叶痴呆-肌萎缩侧索硬化谱系疾病的家族中出现的一种伴有皮质基底节综合征的新型变异(Lys694del):病例报告

A Novel Variant (Lys694del) Presenting With Corticobasal Syndrome in a Family With FTD-ALS Spectrum Diseases: Case Report.

作者信息

Seibert Kaitlin, Smith Heather, Lapins Allison, Pytel Peter, Mastrianni James A

机构信息

Department of Neurology, Center for Comprehensive Care and Research on Memory Disorders, University of Chicago, Chicago, IL, United States.

Department of Pathology, University of Chicago, Chicago, IL, United States.

出版信息

Front Neurol. 2022 Mar 4;13:826676. doi: 10.3389/fneur.2022.826676. eCollection 2022.

Abstract

Several variants of the TANK-Binding Kinase 1 () gene have been associated with frontotemporal dementia - amyotrophic lateral sclerosis (FTD-ALS) spectrum diseases. Corticobasal syndrome (CBS) is characterized by asymmetric limb rigidity, dystonia or myoclonus, in association with speech or limb apraxia, cortical sensory deficit, and/or alien limb. It can result from a variety of underlying pathologies and although typically sporadic, it has been occasionally associated with and variants. We describe here the proband of a family with multiple occurrences of FTD-ALS spectrum disease who developed an isolated right-sided primary asymmetric akinetic-rigid syndrome and subsequent speech and cognitive dysfunction associated with contralateral anterior temporal lobe atrophy on MRI and corresponding hypometabolism by FDG-PET. Genetic testing revealed a novel Lys694del variant of the gene and Type A TDP-43 pathology in a predominantly frontotemporal distribution contralateral to the affected side. To our knowledge this is the first report of CBS as the initial expression of a variant. This case emphasizes the importance of considering genetic screening in patients with CBS, as this may be an underrepresented population on the spectrum of genetic FTD-ALS.

摘要

Tank结合激酶1()基因的几种变体已与额颞叶痴呆-肌萎缩侧索硬化症(FTD-ALS)谱系疾病相关。皮质基底节综合征(CBS)的特征为不对称肢体僵硬、肌张力障碍或肌阵挛,伴有言语或肢体失用、皮质感觉障碍和/或异己肢体现象。它可由多种潜在病理状况引起,虽然通常为散发性,但偶尔也与和变体相关。我们在此描述了一个有多次FTD-ALS谱系疾病发生的家族中的先证者,该先证者出现了孤立的右侧原发性不对称运动不能-强直综合征,随后出现言语和认知功能障碍,MRI显示对侧颞叶前叶萎缩,FDG-PET显示相应部位代谢减低。基因检测发现了该基因一个新的Lys694del变体,且在与患侧相对的主要额颞叶分布区域存在A型TDP-43病理改变。据我们所知,这是首例将CBS作为变体初始表现形式的报告。该病例强调了对CBS患者进行基因筛查的重要性,因为这可能是遗传性FTD-ALS谱系中未得到充分代表的人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f15/8931496/489f6e9dc8ea/fneur-13-826676-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验