重症肌无力的诊断与护理现状。

Duodecim; laaketieteellinen aikakauskirja Pub Date : 2017-01-01

Sari Atula, Kathrin Pfau, Tapani Salmi, Eero Sihvo, Mikko Haapio, Mika Saarela, Mari Auranen

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引用次数: 0

摘要

重症肌无力(MG)是最常见的神经肌肉传递障碍，在用力时引起骨骼肌无力。该病的病程多变，症状和体征可因感染或妊娠而迅速改变。MG是用血清学、电生理和药物工具分类的。准确的诊断有助于选择正确的治疗方法，预测疾病的进程，从而有助于随访。在这篇综述中，我们提出芬兰MG患者的诊断、治疗和随访指南。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Diagnostics and current care of myasthenia gravis.

Myasthenia gravis (MG) is the most common neuromuscular transmission disorder, causing weakness of skeletal muscles on exertion. The course of the disease is highly variable, symptoms and signs may change rapidly due to infection or pregnancy. MG is classified using serological, electrophysiological and pharmaceutical tools. A precise diagnosis allows for the choice of right treatment, predicts the course of disease and hence helps with the follow-up. In this review we present Finnish guidelines for diagnostics, treatment and follow-up of MG patients.

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