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本文引用的文献

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Phenotypic and molecular analyses of primary lateral sclerosis.原发性侧索硬化症的表型和分子分析。
Neurol Genet. 2015 Apr 14;1(1):e3. doi: 10.1212/01.NXG.0000464294.88607.dd. eCollection 2015 Jun.
2
Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.皮质兴奋性变化可区分运动神经元疾病表型与遗传性痉挛性截瘫。
Eur J Neurol. 2015 May;22(5):826-31, e57-8. doi: 10.1111/ene.12669. Epub 2015 Feb 12.
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Cerebro-cerebellar connectivity is increased in primary lateral sclerosis.原发性侧索硬化症患者的脑-小脑连接性增强。
Neuroimage Clin. 2014 Dec 9;7:288-96. doi: 10.1016/j.nicl.2014.12.009. eCollection 2015.
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Extramotor damage is associated with cognition in primary lateral sclerosis patients.在原发性侧索硬化症患者中,运动外损伤与认知功能相关。
PLoS One. 2013 Dec 5;8(12):e82017. doi: 10.1371/journal.pone.0082017. eCollection 2013.
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Resting state functional connectivity alterations in primary lateral sclerosis.原发性侧索硬化症静息态功能连接的改变
Neurobiol Aging. 2014 Apr;35(4):916-25. doi: 10.1016/j.neurobiolaging.2013.09.041. Epub 2013 Oct 12.
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Structural imaging differences and longitudinal changes in primary lateral sclerosis and amyotrophic lateral sclerosis.原发性侧索硬化症和肌萎缩性侧索硬化症的结构影像学差异和纵向变化。
Neuroimage Clin. 2012 Dec 24;2:151-60. doi: 10.1016/j.nicl.2012.12.003. eCollection 2012.
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Imaging findings associated with cognitive performance in primary lateral sclerosis and amyotrophic lateral sclerosis.原发性侧索硬化症和肌萎缩侧索硬化症中与认知表现相关的影像学发现。
Dement Geriatr Cogn Dis Extra. 2013 Aug 16;3(1):233-50. doi: 10.1159/000353456. eCollection 2013.
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Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.遗传性痉挛性截瘫:临床病理特征和新兴分子机制。
Acta Neuropathol. 2013 Sep;126(3):307-28. doi: 10.1007/s00401-013-1115-8. Epub 2013 Jul 30.
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Myelin imaging in amyotrophic and primary lateral sclerosis.肌萎缩侧索硬化症和原发性侧索硬化症的髓鞘成像。
Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):562-73. doi: 10.3109/21678421.2013.794843. Epub 2013 May 16.
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Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases.C9ORF72 中六核苷酸重复扩展与运动神经元病谱。
Neurology. 2012 Aug 28;79(9):878-82. doi: 10.1212/WNL.0b013e3182661d14. Epub 2012 Jul 25.

原发性侧索硬化症

Primary Lateral Sclerosis.

作者信息

Statland Jeffrey M, Barohn Richard J, Dimachkie Mazen M, Floeter Mary Kay, Mitsumoto Hiroshi

机构信息

Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.

Department of Neurology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Mailstop 2012, Kansas City, KS 66160, USA.

出版信息

Neurol Clin. 2015 Nov;33(4):749-60. doi: 10.1016/j.ncl.2015.07.007. Epub 2015 Sep 8.

DOI:10.1016/j.ncl.2015.07.007
PMID:26515619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4628724/
Abstract

Primary lateral sclerosis is characterized by insidious onset of progressive upper motor neuron dysfunction in the absence of clinical signs of lower motor neuron involvement. Patients experience stiffness; decreased balance and coordination; mild weakness; and, if the bulbar region is affected, difficulty speaking and swallowing, and emotional lability. The diagnosis is made based on clinical history, typical examination findings, and diagnostic testing negative for other causes of upper motor neuron dysfunction. Electromyogram is normal, or only shows mild neurogenic findings in a few muscles, not meeting El Escorial criteria. Treatment is largely supportive.

摘要

原发性侧索硬化症的特征是隐匿起病,出现进行性上运动神经元功能障碍,而无下运动神经元受累的临床体征。患者会出现僵硬;平衡和协调能力下降;轻度无力;如果延髓区域受累,则会出现说话和吞咽困难以及情绪不稳定。诊断基于临床病史、典型的检查结果以及针对上运动神经元功能障碍的其他病因的诊断测试呈阴性。肌电图正常,或仅在少数肌肉中显示轻度神经源性改变,不符合埃尔埃斯科里亚尔标准。治疗主要是支持性的。