重症肌无力（MG）是神经肌肉传递系统的自身免疫性疾病，常以眼症或全身性肌无力而发现。
Myasthenia gravis (MG) is an autoimmune disorder of neuromuscular transmission, usually recognized with ocular complaints or generalized muscle weakness.
目的：探讨重症肌无力(MG)危象的诱发因素、延长气管插管的因素以及并发症、病死率。
Object: to discuss the crisis of myasthenia gravis (MG) involving inducement, the factors prolonging tracheal cannula, complications, and fatality rate.
远期并发症为髋关节脱位、脊柱畸形、肌无力。
Late complications included spinal deformity, hip dislocation and hypokinesia.
妊娠并发症的处理过程中应尽量避免加重肌无力的药物，如硫酸镁、氨基糖甙类药物。
Medications which potentiate muscle weakness including magnesium sulfate and aminoglycosides should avoid to be used.
重症肌无力可导致流产、早产、胎膜早破等并发症。
Myasthenia gravis(MG)can lead to abortion, preterm delivery and premature rupture of membranes.
方法回顾性分析了80例重症肌无力患者的发病年龄、发病诱因、临床表现、合并症及治疗效果。
Methods Retrospective analysis on age, clinical feature, treatment and affects were held on 80 patients with MG.
揭示联合用药治疗眼肌型重症肌无力治愈率高，减少了用药量和药物并发症，复发率低，应作为本病的首选治疗方法。
Ocular myopathy myasthenia gravis which had a higher success rate, few complications, lower re1apse rate and may be the first method.
揭示联合用药治疗眼肌型重症肌无力治愈率高，减少了用药量和药物并发症，复发率低，应作为本病的首选治疗方法。
Ocular myopathy myasthenia gravis which had a higher success rate, few complications, lower re1apse rate and may be the first method.
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