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Updated: Aug 14, 2025

Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice
Published on: April 15, 2014
High fever in myelin oligodendrocyte glycoprotein-associated disorder (MOGAD): A diagnostic challenge
Chadi Azar1, Grace Akiki2, Sara F Haddad3
1Department of Internal Medicine and Clinical Immunology, Hotel Dieu de France Hospital, Saint Joseph University, Beirut, Lebanon.
Abstract:
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.
Insights
Myelin oligodendrocyte glycoprotein (MOG)-IgG associated disorders (MOGAD) can present as febrile meningoencephalitis, a rare but challenging diagnosis. Early MOG-IgG testing is crucial for patients with unexplained febrile meningoencephalitis.
Area of Science:
- Neuroimmunology
- Neurology
Background:
- Myelin oligodendrocyte glycoprotein (MOG)-IgG associated disorders (MOGAD) exhibit a widening phenotypic spectrum with increasing recognition of atypical presentations.
- Febrile meningoencephalitis is an uncommon manifestation of MOGAD, posing significant diagnostic challenges.
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