NMOSD和MOGAD诊断和治疗的最新进展

IF 2.4 4区 医学 Q2 CLINICAL NEUROLOGY
Laura Cacciaguerra MD, PhD , Eoin P. Flanagan MB, BCh
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引用次数: 0

摘要

水通道蛋白-4- igg阳性视神经脊髓炎谱系障碍(AQP4+NMOSD)和髓鞘-少突胶质细胞糖蛋白抗体相关疾病(MOGAD)分别是针对星形胶质细胞和少突胶质细胞的抗体相关疾病。它们被认为是不同的实体,导致每一种都有自己的诊断标准,需要结合临床、血清学和MRI特征。AQP4+NMOSD与MOGAD急性发作的治疗方法相似。现在有1类证据支持AQP4+NMOSD的攻击预防药物。尽管临床试验正在进行,但MOGAD缺乏经过证实的治疗方法。在这篇综述中,我们将概述AQP4+NMOSD与MOGAD在诊断和治疗方面的异同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Updates in NMOSD and MOGAD Diagnosis and Treatment
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来源期刊
Neurologic Clinics
Neurologic Clinics 医学-临床神经学
CiteScore
5.00
自引率
4.20%
发文量
92
审稿时长
6-12 weeks
期刊介绍: Targeted toward those in the fields of neurology, family medicine, otolaryngology, and pediatrics, Neurologic Clinics offers a broad view of current practice, as well as the evidence to support it. Published quarterly — in February, May, August, and November — each issue focuses on a single topic neurology, including hearing loss, cholesteatoma, rhinology, anosmia, dysphagia, and pediatric-specific ENT.
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