重症肌无力兰伯特-伊顿重叠综合征:建议修改诊断标准。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Muscle & Nerve Pub Date : 2024-07-28 DOI:10.1002/mus.28221
Shin J Oh
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引用次数: 0

摘要

2016年,MLOS(重症肌无力兰伯特-伊顿重叠综合征)被创造出来,代表重症肌无力和兰伯特-伊顿肌无力综合征重叠综合征的一个实体。目前已发现 55 名 MLOS 患者。建议修改 MG 的诊断标准,增加 MuSK 阳性抗体检测。根据新的诊断标准,发现了两名 MuSK 阳性的 MLOS 患者。
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Myasthenia gravis Lambert-Eaton overlap syndrome: Recommended modification for the diagnostic criteria.

In 2016, MLOS (myasthenia gravis Lambert-Eaton overlap syndrome) was coined to represent an entity of overlap syndrome of myasthenia gravis and Lambert-Eaton myasthenic syndrome. Fifty-five MLOS patients have been identified. Modification of the diagnostic criteria for MG by adding MuSK positive antibody testing is recommended. Two MuSK positive MLOS patients were identified by the new diagnostic criteria.

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来源期刊
Muscle & Nerve
Muscle & Nerve 医学-临床神经学
CiteScore
6.40
自引率
5.90%
发文量
287
审稿时长
3-6 weeks
期刊介绍: Muscle & Nerve is an international and interdisciplinary publication of original contributions, in both health and disease, concerning studies of the muscle, the neuromuscular junction, the peripheral motor, sensory and autonomic neurons, and the central nervous system where the behavior of the peripheral nervous system is clarified. Appearing monthly, Muscle & Nerve publishes clinical studies and clinically relevant research reports in the fields of anatomy, biochemistry, cell biology, electrophysiology and electrodiagnosis, epidemiology, genetics, immunology, pathology, pharmacology, physiology, toxicology, and virology. The Journal welcomes articles and reports on basic clinical electrophysiology and electrodiagnosis. We expedite some papers dealing with timely topics to keep up with the fast-moving pace of science, based on the referees'' recommendation.
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