[Overlapping syndrome of myelin oligodendrocyte glycoprotein-antibody disease and anti-N-methyl-D-aspartate receptor encephalitis in two children]

Zhonghua Er Ke Za Zhi. 2020 Apr 2;58(4):324-326. doi: 10.3760/cma.j.cn112140-20190916-00588.

[Article in Chinese]

Authors

H M Zhu¹, D Sun¹, G F Wu¹, J S Hu¹, Q Q Qian¹, Z S Liu¹

Affiliation

¹ Department of Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430016, China.

PMID: 32234141
DOI: 10.3760/cma.j.cn112140-20190916-00588

Abstract

2例学龄期患儿临床均表现为髓鞘少突胶质细胞糖蛋白（MOG）抗体病后出现抗N-甲基-D-天冬氨酸受体（NMDAR）脑炎，头颅磁共振成像示脱髓鞘病灶以幕上病灶为主，均为复发病程，最后诊断为儿童MOG抗体病合并抗NMDAR脑炎重叠综合征，予以免疫治疗后预后尚可。.

Publication types

Case Reports

MeSH terms

Anti-N-Methyl-D-Aspartate Receptor Encephalitis / diagnosis*
Autoantibodies / blood*
Child
Humans
Myelin-Oligodendrocyte Glycoprotein / immunology*

Substances

Autoantibodies
Myelin-Oligodendrocyte Glycoprotein