医学
视神经炎
横贯性脊髓炎
视神经脊髓炎
髓鞘少突胶质细胞糖蛋白
急性播散性脑脊髓炎
队列
回顾性队列研究
多发性硬化
神经学
脑炎
胃肠病学
内科学
儿科
疾病
病理
免疫学
精神科
病毒
实验性自身免疫性脑脊髓炎
作者
Yi Hua,Xuke Yan,Liu Liu,Yilong Wang,Chaofu Lu,Peifang Jiang,Zhefeng Yuan,Feng Gao
标识
DOI:10.3389/fneur.2023.1188323
摘要
Objective: To analyze the clinical characteristics and follow-up data of children with different clinical phenotypes of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Methods: The basic demographic and clinical features, laboratory and imaging examination results, and follow-up data of 74 Chinese children with different phenotypes of MOGAD were retrospectively reviewed and analyzed. Results: < 0.05). Conclusion: The most common clinical phenotypes of MOGAD in this cohort were ADEM and encephalitis. Recurrence of MOGAD may be related to age and sex, with a higher recurrence rate observed in females. These findings provide a basis for further exploration of the characteristics of different MOGAD phenotypes.
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