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The document reviews the pathophysiology of Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD), highlighting its clinical, radiological, and immunological features. MOGAD presents a spectrum of diseases with distinct characteristics compared to other demyelinating disorders like multiple sclerosis and neuromyelitis optica, particularly in terms of relapse rates and the presence of infectious prodromes. The review emphasizes the role of T cells and MOG antibodies in the disease

Author

Gerardo Fabián Enciso Ark

Language

EN