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Travel Broadens the Mind.旅行开阔眼界。
Infancy. 2000 Apr;1(2):149-219. doi: 10.1207/S15327078IN0102_1. Epub 2000 Apr 1.
2
Motor Performance in Children With Childhood Apraxia of Speech and Speech Sound Disorders.儿童言语运动障碍与语音障碍儿童的运动表现。
J Speech Lang Hear Res. 2019 Sep 20;62(9):3220-3233. doi: 10.1044/2019_JSLHR-S-18-0380. Epub 2019 Sep 3.
3
Altered Connectivity Between Cerebellum, Visual, and Sensory-Motor Networks in Autism Spectrum Disorder: Results from the EU-AIMS Longitudinal European Autism Project.自闭症谱系障碍中海马、视觉和感觉运动网络之间的连通性改变:来自欧盟自闭症纵向项目的结果。
Biol Psychiatry Cogn Neurosci Neuroimaging. 2019 Mar;4(3):260-270. doi: 10.1016/j.bpsc.2018.11.010. Epub 2018 Dec 5.
4
The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature.SCA21(ATX-TMEM240)运动障碍谱:3 个新家族和文献系统回顾。
Parkinsonism Relat Disord. 2019 May;62:215-220. doi: 10.1016/j.parkreldis.2018.11.027. Epub 2018 Nov 29.
5
Lysosomal dysfunction and early glial activation are involved in the pathogenesis of spinocerebellar ataxia type 21 caused by mutant transmembrane protein 240.溶酶体功能障碍和早期神经胶质细胞激活参与了突变跨膜蛋白 240 引起的脊髓小脑性共济失调 21 型的发病机制。
Neurobiol Dis. 2018 Dec;120:34-50. doi: 10.1016/j.nbd.2018.08.022. Epub 2018 Sep 2.
6
Movement Disorders and Syndromic Autism: A Systematic Review.运动障碍与自闭症候群:系统性回顾。
J Autism Dev Disord. 2019 Jan;49(1):54-67. doi: 10.1007/s10803-018-3658-y.
7
Increased foot strike variability in Parkinson's disease patients with freezing of gait.帕金森病冻结步态患者的足部触地方式变异性增加。
Parkinsonism Relat Disord. 2018 Aug;53:58-63. doi: 10.1016/j.parkreldis.2018.04.032. Epub 2018 May 1.
8
Cerebellar contribution to locomotor behavior: A neurodevelopmental perspective.小脑对运动行为的贡献:神经发育的角度。
Neurobiol Learn Mem. 2019 Nov;165:106861. doi: 10.1016/j.nlm.2018.04.016. Epub 2018 Apr 30.
9
A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies.日本 21 型脊髓小脑共济失调家系:临床与神经病理学研究。
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SCA21(ATX-TMEM240)的神经发育和运动表型。

The Neurodevelopmental and Motor Phenotype of SCA21 (ATX-TMEM240).

机构信息

12222David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

8783UCLA Department of Neurology, Program in Neurogenetics, Los Angeles, CA, USA.

出版信息

J Child Neurol. 2020 Dec;35(14):953-962. doi: 10.1177/0883073820943488. Epub 2020 Jul 24.

DOI:10.1177/0883073820943488
PMID:32705938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7674185/
Abstract

Spinocerebellar ataxia type 21 (SCA21/ATX-TMEM240) is a rare form of cerebellar ataxia that commonly presents with motor, cognitive, and behavioral impairments. Although these features have been identified as part of the clinical manifestations of SCA21, the neurodevelopmental disorders associated with SCA21 have not been well studied or described. Here we present extensive phenotypic data for 3 subjects from an SCA21 family in the United States. Genetic testing demonstrated the c.196 G>A (p.Gly66Arg) variant to be a second recurrent mutation associated with the disorder. Standardized developmental assessment revealed significant deficits in cognition, adaptive function, motor skills, and social communication with 2 of the subjects having diagnoses of autism spectrum disorder, which has never been described in SCA21. Quantitative gait analysis showed markedly abnormal spatiotemporal gait variables indicative of poor gait control and cerebellar as well as noncerebellar dysfunction. Clinical evaluation also highlighted a striking variability in clinical symptoms, with greater ataxia correlating with greater severity of neurodevelopmental disorder diagnoses. Notably, neurodevelopmental outcomes have improved with intervention over time. Taken together, this case series identifies that the manifestation of neurodevelopmental disorders is a key feature of SCA21 and may precede the presence of motor abnormalities. Furthermore, the coexistence of ataxia and neurodevelopmental disorders in these subjects suggests a role for spinocerebellar pathways in both outcomes. The findings in this study highlight the importance of evaluation of neurodevelopmental concerns in the context of progressive motor abnormalities and the need for timely intervention to ultimately improve quality of life for individuals with SCA21.

摘要

脊髓小脑性共济失调 21 型(SCA21/ATX-TMEM240)是一种罕见的小脑性共济失调形式,通常表现为运动、认知和行为障碍。尽管这些特征已被确定为 SCA21 临床表现的一部分,但与 SCA21 相关的神经发育障碍尚未得到很好的研究或描述。在这里,我们提供了来自美国一个 SCA21 家族的 3 名受试者的广泛表型数据。基因测试表明 c.196 G>A(p.Gly66Arg)变体是与该疾病相关的第二个复发性突变。标准化发育评估显示,2 名受试者在认知、适应功能、运动技能和社会交流方面存在显著缺陷,其中 2 名被诊断为自闭症谱系障碍,这在 SCA21 中从未被描述过。定量步态分析显示,时空步态变量明显异常,表明步态控制不佳以及小脑和非小脑功能障碍。临床评估还突出了临床症状的显著变异性,共济失调越严重,神经发育障碍的诊断越严重。值得注意的是,随着时间的推移,神经发育结局通过干预得到改善。综上所述,本病例系列研究表明,神经发育障碍的表现是 SCA21 的一个关键特征,并且可能早于运动异常的出现。此外,这些受试者中共济失调和神经发育障碍的共存表明,脊髓小脑途径在这两种结果中都起作用。本研究的结果强调了在进行性运动异常的背景下评估神经发育问题的重要性,以及及时干预以最终提高 SCA21 患者生活质量的必要性。