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重症肌无力 (ＭＧ)是主要累及神经肌肉接头处突触后膜上乙酰胆碱受体 (ＡｃｈＲ)的 ,由乙酰胆碱受体抗体 (ＡｃｈＲ Ａｂ)介导 ,细胞免疫依赖性、补体参与的自身免疫性疾病[1] 。1 ＭＧ分型成人ＭＧ与儿童ＭＧ的Ｏｓｓｅｒｍａｎ分型法分型有所不同。成人ＭＧ常采用改良Ｏｓｓ
Myasthenia Gravis (MG) is an autoimmune disease mainly involving the acetylcholine receptor (AchR) on the postsynaptic membrane at the neuromuscular junction, mediated by the acetylcholine receptor antibody (AchR Ab), cellular immunity, complement [1] . 1 MG genotyping Adult MG and children MG Osserman typing type is different. Adult often use modified Oss MG