视神经脊髓炎
髓鞘少突胶质细胞糖蛋白
多发性硬化
医学
光谱紊乱
脱髓鞘病
免疫学
抗体
鞘内
水通道蛋白4
疾病
脱髓鞘病
病理
精神科
外科
实验性自身免疫性脑脊髓炎
作者
Yael Hacohen,Wesley T. Kerr,Patrick Waters
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2021-07-06
卷期号:97 (1): 12-13
被引量:4
标识
DOI:10.1212/wnl.0000000000012177
摘要
Myelin oligodendrocyte glycoprotein (MOG) antibody (Ab)–associated disease (MOGAD) is now a well-recognized demyelinating disease. Despite the phenotypic overlap with both multiple sclerosis and aquaporin-4 (AQP4)-Ab neuromyelitis optica spectrum disorder, cumulative clinical and immunologic evidence clearly discriminates between these conditions.
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