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伴有完全性传导阻滞的肥厚性神经病——遗传性运动和感觉神经病III型

Hypertrophic neuropathy with complete conduction block-- hereditary motor and sensory neuropathy type III.

作者信息

Yim S Y, Lee I Y, Moon H W, Rah U W, Kim S H, Shim C, Joo H J

机构信息

Department of Rehabilitation Medicine, Ajou University School of Medicine, Suwon, Korea.

出版信息

Yonsei Med J. 1995 Nov;36(5):466-72. doi: 10.3349/ymj.1995.36.5.466.

Abstract

Hypertrophic neuropathy is a non-specific consequence of repeated demyelination and remyelination, encountered in a wide range of inherited and acquired disorders. We report an 11-year-old boy with HMSN III, a kind of hypertrophic neuropathy, with clinical, electrophysiologic and pathologic data. The electrophysiologic studies show complete conduction block in the upper and lower extremities with severe abnormal spontaneous activities. The pathologic findings of sural nerve reveal prominent hypomyelination, onion bulb formation, and severe endoneurial collagenization. Complete conduction block with the preservation of fair to good grade muscle strength is an unusual finding in hypertrophic neuropathy and other peripheral neuropathies, in general.

摘要

肥厚性神经病变是反复脱髓鞘和再髓鞘化的非特异性结果,见于多种遗传性和获得性疾病。我们报告一名患有遗传性运动感觉神经病III型(一种肥厚性神经病变)的11岁男孩,并提供其临床、电生理和病理数据。电生理研究显示上下肢完全性传导阻滞,伴有严重异常自发电活动。腓肠神经的病理结果显示明显的髓鞘形成不足、洋葱球样结构形成和严重的神经内膜胶原化。在肥厚性神经病变及其他周围神经病变中,一般来说,存在完全性传导阻滞但肌肉力量仍保持良好或中等程度是不寻常的表现。

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