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莱氏病中的周围神经病变

Peripheral neuropathy in Leigh's disease.

作者信息

Jacobs J M, Harding B N, Lake B D, Payan J, Wilson J

机构信息

Institute of Neurology, National Hospital, Queen Square, London.

出版信息

Brain. 1990 Apr;113 ( Pt 2):447-62. doi: 10.1093/brain/113.2.447.

Abstract

Sural nerves were examined in 3 childhood cases of Leigh's disease (from 2 families), each with electrophysiological documentation of peripheral neuropathy. Postmortem confirmation of Leigh's disease was made in 2 cases; the third had characteristic CT scan appearances. Myelinated fibre densities were within normal limits, with no evidence of degeneration or regeneration. The myelin sheaths, however, appeared thin and this was confirmed quantitatively. In teased fibres there was no demyelination in 2 cases but some in 1 case. The findings suggest that there is hypomyelination of peripheral nerves leading eventually to demyelination.

摘要

对3例儿童 Leigh 病患者(来自2个家庭)的腓肠神经进行了检查,每例均有周围神经病变的电生理记录。2例经尸检确诊为 Leigh 病;第3例有典型的CT扫描表现。有髓纤维密度在正常范围内,无变性或再生迹象。然而,髓鞘看起来很薄,这一点得到了定量证实。在 teased 纤维中,2例未发现脱髓鞘,但1例有脱髓鞘现象。这些发现提示周围神经存在髓鞘形成不足,最终导致脱髓鞘。

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