Severe MOG Antibody-Associated Encephalitis in Children: Clinical Features, Diagnostic Challenges, and Immunotherapy Escalation – A Practical Review
DOI:
https://doi.org/10.48047/v7x1kw18Keywords:
Myelin oligodendrocyte glycoprotein antibody–associated disease, EncephalitisAbstract
Background: Myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) has emerged as a distinct autoimmune
neuroinflammatory disorder in childhood, characterized by a wide clinical spectrum ranging from monophasic acute disseminated
encephalomyelitis to recurrent optic neuritis a
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References
Di Pauli F, Berger T. Myelin oligodendrocyte glycoprotein antibody-associated disorders: clinical phenotypes and diagnostic challenges. Curr Opin Neurol. 2018;31(3):289-295.
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