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重症肌无力(myasthenia gravis,MG)是一种以神经肌肉接头传导障碍为特征的自身免疫性疾病,眼外肌常首先受累[1],临床上分为眼肌型(ocular MG,OMG)和全身型(general MG,GMG)。有报道显示MG致死率已降至5%以下,存活者基本可享受正常预期寿命
Myasthenia gravis (MG) is an autoimmune disease characterized by neuromuscular junction conduction disorder. Extraocular muscles are often first involved [1] and are clinically divided into ocular MG (OMG) and General MG (GMG). It has been reported that the lethality of MG has dropped below 5%, and the survivors can enjoy the normal life expectancy