重症肌无力
发病机制
医学
抗体
耐火材料(行星科学)
疾病
萎缩
耐火期
免疫学
胃肠病学
内科学
生物
天体生物学
出处
期刊:PubMed
日期:2024-01-01
卷期号:76 (1): 47-53
标识
DOI:10.11477/mf.1416202557
摘要
Long-term remission is rare in patients with myasthenia gravis (MG), and health-related quality of life is lower in patients with MG than in healthy individuals. Approximately 5% of patients with MG show positive results on muscle-specific kinase (MuSK) antibody testing and usually have severe symptoms, refractory disease, residual muscle atrophy, and poor prognosis. Recent studies that have investigated the pathogenesis of MuSK antibody-positive MG have reported contributors to treatment refractoriness in cases of MG. In this article, we review the most recent findings.
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