Suppr超能文献

家族性交叉条纹灶性缺失

Familial focal loss of cross striations.

作者信息

van Wijngaarden G K, Bethlem J, Dingemans K P, Coërs C, Telerman-Toppet N, Gérard J M

出版信息

J Neurol. 1977 Oct 7;216(3):163-72. doi: 10.1007/BF00313617.

Abstract

Two patients, a brother and sister, both suffering from congenital generalized muscle weakness with a progressive course are reported. Muscle biopsy revealed areas with loss of cross striations in the muscle fibers, electronmicroscopically presenting complete disorganization of the myofibrils with streaming of the Z discs and absence of mitochondria. Vesicular nuclei with prominent nucleoli were present in these areas. There was a type I fiber predominance in both cases. The mean diameter of the type I muscle fibers in one of the cases was too small. Motor endplate alterations in this patient gave no evidence of denervation but were suggestive of a delayed development of motor nerves.

摘要

报告了两名患者,为兄妹,均患有先天性全身肌无力,病情呈进行性发展。肌肉活检显示肌纤维横纹消失区域,电镜下可见肌原纤维完全紊乱,Z线移位,线粒体缺失。这些区域存在泡状核,核仁明显。两例均以I型纤维为主。其中一例患者I型肌纤维的平均直径过小。该患者运动终板改变未显示去神经支配迹象,但提示运动神经发育延迟。

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