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脊髓灰质炎及其他神经源性肌肉萎缩后晚期运动神经元变性的线粒体异常。

Mitochondrial abnormalities of late motor neuron degeneration following poliomyelitis and other neurogenic muscular atrophies.

作者信息

Schiffer D, Palmucci L, Bertolotto A, Monga G

出版信息

J Neurol. 1979 Sep;221(3):193-201. doi: 10.1007/BF00313051.

Abstract

A case of late motor neuron degeneration following poliomyelitis with abnormal mitochondria in muscle fibers is presented with two additional cases of systemic neurogenic muscular atrophy (Charcot-Marie-Tooth disease). Muscle biopsy revealed a neurogenic pattern of variable severity in all cases. Subsarcolemmal zones of hyperactivity and hyperpositive intermyofibrillar collections of granular material present in a variable proportion of type I fibers were demonstrated by oxidative enzymes. Ultrastructurally they corresponded to abnormal mitochondria, with paracrystalline inclusions in one case. The finding is discussed in the light of the previous literature on mitochondrial myopathies. Mitochondrial alterations are not specific and their significance in neurogenic conditions is debated.

摘要

本文报告1例脊髓灰质炎后迟发性运动神经元变性伴肌纤维线粒体异常的病例,以及另外2例系统性神经源性肌肉萎缩(夏科-马里-图斯病)的病例。所有病例的肌肉活检均显示出严重程度各异的神经源性模式。氧化酶显示,在不同比例的I型纤维中存在肌膜下高活性区和肌原纤维间颗粒物质的高阳性聚集。超微结构显示它们对应于异常线粒体,其中1例有线状晶体包涵体。结合先前关于线粒体肌病的文献对这一发现进行了讨论。线粒体改变并非特异性的,其在神经源性疾病中的意义存在争议。

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