论文部分内容阅读
重症肌无力(myasthenia gravis,MG)是神经肌肉接头(neuromuscular junction,NMJ)的自身免疫病,表现为波动性肌无力症状,亦可有较恒定的体征[1]。MG可累及全身骨骼肌,亦可累及平滑肌和心肌,受累肌群的不同使症状丰富多样。其首发症状缺乏特异性,患者肌群运用情况不同也使发现症?
Myasthenia gravis (MG) is an autoimmune disease of the neuromuscular junction (NMJ), which manifests as a condition of fluctuating myasthenia gravis and may have a more constant sign [1]. MG can affect the body’s skeletal muscle, but also affect the smooth muscle and myocardium, involving different muscle groups so that the rich and varied symptoms. The lack of specificity of the first symptom, the use of patients with different muscle groups also found that disease?