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- W2949772242 abstract "A subset of patients with neuromyelitis optica spectrum disorders are positive for myelin-oligodendrocyte glycoprotein (MOG) antibodies. These patients present with distinct clinical demyelinating syndrome often confused for multiple sclerosis. We describe the case of a patient who initially presented with 10-day history of right-sided retro-orbital headache worse with lateral gaze, photophobia, and subjective decreased visual acuity. After successful treatment on a steroid regimen, this patient represented two weeks following discharge with seizure and was found to have unilateral meningeal T2-FLAIR MRI hyperintensity with associated cortical swelling, a rare finding. CSF studies showed negative anti-AQP4 antibodies and positive anti-MOG antibodies. This case demonstrates that patients presenting with symptoms concerning for NMOSD who are AQP4-Ab-negative should be tested for anti-MOG antibodies for optimized disease management and important prognostic implications." @default.
- W2949772242 created "2019-06-27" @default.
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- W2949772242 date "2019-09-01" @default.
- W2949772242 modified "2023-09-30" @default.
- W2949772242 title "Optic neuritis, encephalitis and leptomeningeal enhancement in a patient with anti-MOG antibodies: A case study" @default.
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- W2949772242 doi "https://doi.org/10.1016/j.msard.2019.06.010" @default.
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