难治性重症肌无力-患者负担和对新治疗靶点的需求

Q4 Medicine
S. Jacob
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引用次数: 2

摘要

重症肌无力(MG)是一种以肌肉无力和疲劳为特征的自身免疫性疾病。症状包括口齿不清,四肢无力,吞咽和呼吸困难,这可能导致危及生命的肌无力危机。尽管接受了推荐的治疗,但许多MG患者报告健康相关的生活质量很低,主要是由于活动能力受损和抑郁。此外,大约10%的广泛性MG患者对治疗没有反应。难治性MG患者的生活质量严重受损,对这组患者进行新的治疗评估是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Refractory Myasthenia Gravis – Patient Burden and the Need for New Therapeutic Targets
Myasthenia gravis (MG) is an autoimmune disorder characterised by muscle weakness and fatigue. Symptoms include slurred speech, weakness in the arms and legs and difficulty swallowing and breathing, which can lead to life-threatening myasthenic crisis. Despite receiving recommended therapies, many patients with MG report health-related quality of life is low, largely due to impaired mobility and depression. Furthermore, around 10% of patients with generalised MG fail to respond to treatment. Patients with refractory MG have a severely compromised quality of life and it is important that new treatments are evaluated for this group of patients.
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来源期刊
European neurological review
European neurological review Medicine-Neurology (clinical)
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