Suppr超能文献

先天性肌强直患者发生重症肌无力。

Occurrence of myasthenia gravis in a patient with congenital myotonia.

作者信息

Matsumoto H, Sugiyama T, Ito M, Yachi A

出版信息

J Neurol Sci. 1982 Nov-Dec;57(1):83-8. doi: 10.1016/0022-510x(82)90112-5.

Abstract

Myasthenia gravis developed acutely in a 32-year-old woman, who incidentally was found to have myotonia congenita of the autosomal dominant mode of inheritance. The simultaneous occurrence of myasthenia gravis and myotonia congenita was established clinically, pharmacologically and electromyographically. There was no immunologic abnormality, whereas the thymus was detected by pneumomediastinographic tomograms. About 2 months after the onset of myasthenia gravis, thymectomy was performed resulting in progressive improvement of myasthenia without apparent change in the myotonia.

摘要

一名32岁女性急性发生重症肌无力,偶然发现其患有常染色体显性遗传模式的先天性肌强直。重症肌无力和先天性肌强直的同时出现通过临床、药理学和肌电图检查得以确诊。不存在免疫异常,而通过纵隔充气造影断层扫描检测到胸腺。重症肌无力发病约2个月后进行了胸腺切除术,结果重症肌无力逐渐改善,而肌强直无明显变化。

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