肌萎缩侧索硬化症的神经生理学诊断

Q4 Medicine
Claas Janssen, Susanne Petri, Katja Kollewe
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引用次数: 0

摘要

肌萎缩性侧索硬化症(ALS)是一种进行性神经退行性疾病,导致运动皮层和前角的运动神经元破坏。对于ALS的诊断,迄今为止还没有可靠的生物标志物。诊断依据临床检查和神经生理诊断。因此,神经生理检查对ALS的诊断和鉴别诊断具有决定性作用。在接下来的研究中,介绍了在ALS诊断中建立的神经生理检查(神经电图、肌电图和诱发电位),并简要展望了运动单位数指数和肌肉超声检查等ALS领域中有前途的新检查技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurophysiologische Diagnostik der Amyotrophen Lateralsklerose

Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disease leading to the destruction of the motoneurons in the motor cortex and in the anterior horn. For the diagnosis of ALS, no reliable biomarker is available to date. The diagnosis is based on clinical examination and neurophysiological diagnostics.

The neurophysiological examination thus plays a decisive role in the diagnosis of ALS and its differential diagnosis. In the following study, the neurophysiological investigations (electroneurography, electromyography, and evoked potentials) established in ALS diagnostics are presented and a brief outlook on promising newer investigation techniques in the field of ALS such as Motor Unit Number Index and Muscle ultrasonography are given.

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来源期刊
Neurophysiologie-Labor
Neurophysiologie-Labor Medicine-Pathology and Forensic Medicine
CiteScore
0.20
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