马德拉斯型运动神经元病中上运动神经元延迟局灶累及

R Massa , A Scalise , C Iani , M.G Palmieri , G Bernardi
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引用次数: 13

摘要

我们报告的情况下,一个年轻的男子从印度南部,最初提出良性单一肌萎缩症(BMA)的典型征象在左上肢。几年后,其他肢体的受累和球征的出现表明可能诊断为马德拉斯运动神经元病(MMND)。串行运动诱发电位(MEP)记录允许检测上运动神经元(UMN)在原肌萎缩肢体中控制神经支配的局灶性受累的开始。因此,连续MEP记录可用于早期发现以纯下运动神经元(LMN)体征为表现的运动神经元疾病的亚临床UMN损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease

We report the case of a young man from the south of India, initially presenting the typical signs of benign monomelic amyotrophy (BMA) in the left upper limb. After several years, the involvement of other limbs and the appearance of bulbar signs suggested the possible diagnosis of the Madras pattern of motor neuron disease (MMND). Serial motor evoked potential (MEP) recordings allowed detection of the onset of a focal involvement of upper motor neurons (UMN) controlling innervation in the originally amyotrophic limb. Therefore, serial MEP recordings can be useful for the early detection of sub-clinical UMN damage in motor neuron disease presenting with pure lower motor neuron (LMN) signs.

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