重症肌无力

James M Gilchrist MD
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引用次数: 0

摘要

重症肌无力是一种自身免疫性疾病,由针对神经肌肉接点乙酰胆碱受体的抗体引起,导致骨骼肌疲劳无力。对中枢胆碱能通路和神经心理功能的影响存在争议。本文将回顾重症肌无力的诊断,包括临床、历史、药理学、电诊断和免疫学方法,以及症状性和免疫抑制性重症肌无力的治疗。各种药物对重症肌无力的影响也将被审查,以帮助防止无意的急性加重或揭露疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myasthenia Gravis

Myasthenia gravis is an autoimmune disease caused by antibodies directed against the acetylcholine receptor at the neuromuscular junction, resulting in fatigable weakness of skeletal muscles. Effects on central cholinergic pathways and neuropsychologic function are controversial. This article will review the diagnosis of myasthenia gravis, using clinical, historical, pharmacologic, electrodiagnostic, and immunologic methods, and the treatment of myasthenia, both symptomatic and immunosuppressive. The effect of various medications on myasthenia gravis will also be reviewed to help prevent inadvertant acute exacerbation or unmasking of the disease.

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