High fever in myelin oligodendrocyte glycoprotein-associated disorder (MOGAD): A diagnostic challenge

The phenotypic spectrum of myelin oligodendrocyte glycoprotein (MOG)-IgG associated disorders (MOGAD) has broadened in the past few years, and atypical phenotypes are increasingly recognized. Febrile meningoencephalitis has rarely been reported as a feature of MOGAD and represents a diagnostic chall...

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Veröffentlicht in:Multiple sclerosis journal - experimental, translational and clinical translational and clinical, 2023-01, Vol.9 (1), p.20552173221148911
Hauptverfasser: Azar, Chadi, Akiki, Grace, Haddad, Sara F, Kerbage, Anthony, Haddad, Fady, Macaron, Gabrielle
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container_title Multiple sclerosis journal - experimental, translational and clinical
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creator Azar, Chadi
Akiki, Grace
Haddad, Sara F
Kerbage, Anthony
Haddad, Fady
Macaron, Gabrielle
description The phenotypic spectrum of myelin oligodendrocyte glycoprotein (MOG)-IgG associated disorders (MOGAD) has broadened in the past few years, and atypical phenotypes are increasingly recognized. Febrile meningoencephalitis has rarely been reported as a feature of MOGAD and represents a diagnostic challenge. We report the case of 24-year-old women with high-grade fever, meningoencephalomyelitis, and persistently positive MOG-IgG, for whom an extensive infectious work-up was negative and who responded to high-dose intravenous methylprednisolone. The full clinical spectrum of MOGAD is yet to be completely elucidated. In patients presenting with febrile meningoencephalitis, MOG-IgG testing should be considered particularly if infectious work-up is negative.
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subjects Case Report
Encephalitis
Fever
Genotype & phenotype
Glycoproteins
Medical diagnosis
Meningitis
title High fever in myelin oligodendrocyte glycoprotein-associated disorder (MOGAD): A diagnostic challenge
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