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Myasthenia gravis
Myasthenia gravis (MG) is an autoimmune disease with conduction disorders at the skeletal muscle neuromuscular junction. It is characterized by muscle fatigue that is mild in the morning and severe in the evening, and is relieved after rest or taking cholinesterase inhibitors. It often affects the extraocular muscles, masticatory muscles, swallowing muscles, and respiratory muscles. In severe cases, the bulbar palsy occurs. The distribution of affected muscles varies from person to person and from time to time, and it is not a paralysis that occurs when a certain nerve is damaged. This disease should be called acquired autoimmune myasthenia gravis, usually referred to as myasthenia gravis.
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Indication: Anticholinesterase drugs. Used to antagonize the residual muscle relaxant effect of non-depolarizing muscle relaxants at the end of surgery, and used for myasthenia gravis, postoperative functional intestinal flatulence and urinary retention, etc.
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Indication: Anticholinesterase drugs. Used to antagonize the residual muscle relaxant effect of non-depolarizing muscle relaxants at the end of surgery, and used for myasthenia gravis, postoperative functional intestinal flatulence and urinary retention, etc.
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