Clinical Course, Imaging Characteristics, and Therapeutic Response in Myelin Oligodendrocyte Glycoprotein Antibody Disease: A Case Series

Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a novel central nervous system autoimmune disorder which forms part of aquaporin 4 (AQP-4) negative, neuromyelitis optica (NMO) spectrum disorder. It has a distinct clinical profile, neuroimaging features and courses from AQP-4 positive N...

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Veröffentlicht in:	Journal of neurosciences in rural practice 2020-01, Vol.11 (1), p.205-210, Article 205
Hauptverfasser:	James, Joe, Jose, James, Gafoor, V Abdul, Smita, B, Balaram, Neetha, Ramachandran, Aparna
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Series
Online-Zugang:	Volltext
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Zusammenfassung:	Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a novel central nervous system autoimmune disorder which forms part of aquaporin 4 (AQP-4) negative, neuromyelitis optica (NMO) spectrum disorder. It has a distinct clinical profile, neuroimaging features and courses from AQP-4 positive NMO and multiple sclerosis. This article is a case series of six patients with MOG antibody disease with longitudinal follow-up for up to 8 months.
ISSN:	0976-3147 0976-3147 0976-3155
DOI:	10.1055/s-0040-1701371