15 July 2024
: Case report 
Optic Neuritis Leading to Vision Loss: A Case of MOG-Associated Disease with Successful Immunotherapy
Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Unexpected drug reaction, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
Meng-meng WangACEFG, Tao HuangABCDEF, Jia-xun LiACD, Yang YaoABC, Ying ChenABC, Kai-kai FuABD, Wen-rong MiaoBCD, Yi HanACDFGDOI: 10.12659/AJCR.943112
Am J Case Rep 2024; 25:e943112
Figure 4. Cranial magnetic resonance imaging (MRI) of a 42-year-old woman with positive antibody testing for myelin oligodendrocyte glycoprotein (MOG) at follow-ups. There were no significant abnormalities after 1 month (A) and after 6 months (B). MOG – myelin oligodendrocyte glycoprotein; MRI – magnetic resonance imaging.