与线粒体肌病相关的周围神经病变。

Australian paediatric journal Pub Date : 1988-01-01
C Yiannikas, J G McLeod, J D Pollard, J Baverstock
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引用次数: 0

摘要

研究了20例线粒体肌病患者是否存在周围神经病变。5例(25%)患者有轻度感觉运动神经病变的临床表现,10例(50%)患者神经传导检查异常。电生理研究显示,与对照组相比,整个组的运动和感觉传导明显受损。对4例临床神经病变患者进行腓肠神经活检和形态计量学研究。有髓纤维密度降低,有髓纤维和无髓纤维轴突变性的电镜特征明显。在两条神经的许旺细胞细胞质中可见含有旁晶包涵体的异常线粒体。
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Peripheral neuropathy associated with mitochondrial myopathy.

Twenty patients with mitochondrial myopathy were investigated for the presence of peripheral neuropathy. There were clinical features of a mild sensorimotor neuropathy in five patients (25%) and nerve conduction studies were abnormal in 10 patients (50%). Electrophysiological studies of the whole group showed significant impairment of motor and sensory conduction compared with controls. Sural nerve biopsy and morphometric studies were performed on four patients with clinical neuropathy. There was a reduction in density of myelinated fibres and electron microscopic features of axonal degeneration affecting myelinated and unmyelinated fibres were in evidence. Abnormal mitochondria containing paracrystalline inclusions were seen in the Schwann cell cytoplasm of two nerves.

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