重症肌无力患者围术期麻醉管理的进展
摘要
重症肌无力(myasthenia gravis,MG)是一种由抗体介导的乙酰胆碱(Ach)受体(AchR)受损和功能性AchR减少的自身免疫性疾病,其临床特征是骨骼肌无力和易疲劳,活动后症状加重,休息或予胆碱酯酶抑制剂治疗后可缓解。
出处
《上海医学》
CAS
CSCD
北大核心
2015年第4期331-335,共5页
Shanghai Medical Journal
基金
安徽省卫生厅医学科研项目资助(2010C066)
参考文献35
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