视神经炎
医学
视神经脊髓炎
髓鞘少突胶质细胞糖蛋白
光谱紊乱
皮肤病科
多发性硬化
疾病
少突胶质细胞
髓鞘
病理
免疫学
精神科
中枢神经系统
内科学
实验性自身免疫性脑脊髓炎
作者
Sabrina Poonja,Natthapon Rattanathamsakul,John J. Chen
标识
DOI:10.1097/wco.0000000000001335
摘要
The purpose of this article is to provide a review of neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), with a focus on what renders optic neuritis "atypical" in these two conditions. Clinical features, diagnostic criteria, and epidemiology are outlined. Acute treatments for optic neuritis, as well as immunotherapy for NMOSD and MOGAD are discussed.
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