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Clinical characteristics and outcomes of patients with overlapping Miller Fisher syndrome and myasthenia gravis

机译:Miller Fisher综合征和重症肌无力重叠患者的临床特征和预后

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摘要

Myasthenia gravis (MG) is an autoimmune disease characterized by muscle weakness and fatigue, which is caused by autoantibodies directed against acetylcholine receptors (AChR) at the neuromuscular junction [ ]. The prognosis is relatively favorable with optimum symptomatic, immunosuppressive and supportive treatment. Pyridostigmine is the preferred symptomatic treatment, and corticosteroids, azathioprine and thymectomy are first-line immunosuppressive therapies [ ].
机译:重症肌无力(MG)是一种以肌肉无力和疲劳为特征的自身免疫性疾病,由神经肌肉接头处针对乙酰胆碱受体(AChR)的自身抗体引起。最佳的对症治疗,免疫抑制和支持治疗预后相对较好。吡啶斯的明是首选的对症治疗,而皮质类固醇,硫唑嘌呤和胸腺切除术是一线免疫抑制疗法[]。

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