髓鞘少突胶质细胞糖蛋白
糖蛋白
抗体
队列
髓鞘
少突胶质细胞
医学
疾病
免疫学
病理
生物
内科学
分子生物学
中枢神经系统
作者
Aviv Fineberg,Itay Lotan,Omer Bialer,Alon Tiosano,Shira Rozenblatt,Adi Wilf‐Yarkoni,Mark A. Hellmann,Hadas Stiebel‐Kalish
出处
期刊:PubMed
日期:2024-08-01
卷期号:26 (7): 434-440
摘要
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a rare autoimmune demyelinating disorder of the central nervous system. Optic neuritis (ON) is the most common clinical manifestation of MOGAD in adults. In 2023, new MOGAD diagnostic criteria were proposed, highlighting the importance of supplemental criteria when MOG-immunoglobulin G (IgG) titers are unavailable.
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