Suppr超能文献

遗传性运动和感觉神经病I型中相对于髓鞘螺旋长度的细轴突。

Thin axons relative to myelin spiral length in hereditary motor and sensory neuropathy, type I.

作者信息

Nukada H, Dyck P J, Karnes J L

出版信息

Ann Neurol. 1983 Dec;14(6):648-55. doi: 10.1002/ana.410140608.

Abstract

The relationship of axonal to myelin area in semithin transverse sections of myelinated fibers obtained from sural nerves at the ankle level was morphometrically assessed using computer imaging. Ten patients with hereditary motor and sensory neuropathy, type I and 41 control subjects were examined. In large- and intermediate-diameter myelinated fibers of diseased nerves, axons were significantly attenuated relative to the amount of myelin. Using electron micrographs, a similar finding was obtained when axon area was regressed on myelin spiral length. The altered relationship was found to be greater with more severe fiber loss. These data, plus other evidence, indicate that in this disorder there is a progressive atrophy of axons, usually most severe in distal aspects of lumbosacral neurons and associated with secondary segmental demyelination and remyelination and hypertrophic neuropathy, preceding distal axonal loss. Because the process may begin in utero or in infancy, not only atrophy but also maldevelopment of axons may be involved.

摘要

利用计算机成像技术,对从踝关节水平的腓肠神经获取的有髓纤维半薄横切片中轴突与髓鞘面积的关系进行了形态计量学评估。研究了10例I型遗传性运动和感觉神经病患者以及41名对照者。在患病神经的大直径和中等直径有髓纤维中,相对于髓鞘量,轴突明显变细。使用电子显微镜照片,当轴突面积与髓鞘螺旋长度进行回归分析时,也得到了类似的结果。发现纤维丢失越严重,这种改变的关系就越明显。这些数据以及其他证据表明,在这种疾病中,轴突会进行性萎缩,通常在腰骶神经元的远端最为严重,并伴有继发性节段性脱髓鞘和再髓鞘化以及肥厚性神经病,先于远端轴突丢失。由于这个过程可能在子宫内或婴儿期就开始了,所以不仅涉及轴突萎缩,还可能涉及轴突发育不良。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验