神经肌肉超声在肌萎缩侧索硬化症中的临床和研究应用

IF 2.1 Q3 CLINICAL NEUROLOGY
Degenerative neurological and neuromuscular disease Pub Date : 2019-07-16 eCollection Date: 2019-01-01 DOI:10.2147/DNND.S215318
Stephanie L Barnes, Neil G Simon
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引用次数: 0

摘要

摘要肌萎缩侧索硬化症(ALS)是一种破坏性的神经退行性疾病,其特征是多个神经轴水平的功能障碍。它仍然是一种临床诊断,没有明确的诊断调查。电诊断测试提供了支持性信息,与成像和生物化学标记物一起,可以帮助排除模拟条件。神经肌肉超声在ALS的诊断和监测中具有重要作用,为临床评估和电诊断测试以及对该疾病潜在病理生理学的深入了解提供了补充信息。这篇综述强调了超声在评估ALS的延髓、四肢和呼吸肌肉组织以及周围神经方面的证据。需要在这一不断发展的领域进行进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and research applications of neuromuscular ultrasound in amyotrophic lateral sclerosis.

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder characterized by dysfunction at multiple levels of the neuraxis. It remains a clinical diagnosis without a definitive diagnostic investigation. Electrodiagnostic testing provides supportive information and, along with imaging and biochemical markers, can help exclude mimicking conditions. Neuromuscular ultrasound has a valuable role in the diagnosis and monitoring of ALS and provides complementary information to clinical assessment and electrodiagnostic testing as well as insights into the underlying pathophysiology of this disease. This review highlights the evidence for ultrasound in the evaluation of bulbar, limb and respiratory musculature and peripheral nerves in ALS. Further research in this evolving area is required.

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