Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: A Diverse Demyelinating Entity in Pediatric Patients

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is an autoimmune demyelinating disorder characterized by antibodies targeting the myelin oligodendrocyte glycoprotein, a protein of the myelin sheath in the central nervous system. Increasingly recognized as a distinct clinical entity, MOGAD requires tailored treatment strategies and careful long-term monitoring, rather than being considered a variant of multiple sclerosis and neuromyelitis optica spectrum disorder. While acute episodes respond well to immunotherapy, relapses are common and require long-term management. Progress in immune-based and remyelination therapies offers hope for improving outcomes.

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Publication Details

Journal
Al-Rafidain Journal of Medical Sciences ( ISSN 2789-3219 )
Published
2025-10-02
DOI
https://doi.org/10.54133/ajms.v9i2.2297
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: A Diverse Demyelinating Entity in Pediatric Patients

Mushriq Abdullah Hussein, Basma Adel Ibrahim, Wasnaa Hadi Abdullah, Rasha Sulaiman Abdulraheem
Al-Rafidain Journal of Medical Sciences ( ISSN 2789-3219 )
Multiple Sclerosis Research Studies
article

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: A Diverse Demyelinating Entity in Pediatric Patients

Mushriq Abdullah Hussein, Basma Adel Ibrahim, Wasnaa Hadi Abdullah, Rasha Sulaiman Abdulraheem
article en

Abstract

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is an autoimmune demyelinating disorder characterized by antibodies targeting the myelin oligodendrocyte glycoprotein, a protein of the myelin sheath in the central nervous system. Increasingly recognized as a distinct clinical entity, MOGAD requires tailored treatment strategies and careful long-term monitoring, rather than being considered a variant of multiple sclerosis and neuromyelitis optica spectrum disorder. While acute episodes respond well to immunotherapy, relapses are common and require long-term management. Progress in immune-based and remyelination therapies offers hope for improving outcomes.

Al-Rafidain Journal of Medical Sciences ( ISSN 2789-3219 )Vol. 9(2)
Mustansiriyah University (IQ)
Openalex Percentile: Top 62%
Multiple Sclerosis Research Studies
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