Clinical and Radiological Features of Myelin Oligodendrocyte Glycoprotein-Associated Myelitis in Adults.
demyelinating diseases
multiple sclerosis
myelin oligodendrocyte glycoprotein
myelitis
neuromyelitis optica spectrum disorder
Journal
Journal of clinical neurology (Seoul, Korea)
ISSN: 1738-6586
Titre abrégé: J Clin Neurol
Pays: Korea (South)
ID NLM: 101252374
Informations de publication
Date de publication:
May 2022
May 2022
Historique:
received:
05
01
2022
revised:
14
02
2022
accepted:
14
02
2022
entrez:
19
5
2022
pubmed:
20
5
2022
medline:
20
5
2022
Statut:
ppublish
Résumé
Antibodies against myelin oligodendrocyte glycoprotein (MOG-IgG) have recently been established as a biomarker for MOG-antibody-associated disease (MOGAD), which is a distinct demyelinating disease of the central nervous system. Among the diverse clinical phenotypes of MOGAD, myelitis is the second-most-common presentation in adults, followed by optic neuritis. While some features overlap, there are multiple reports of distinctive clinical and radiological features of MOG-IgG-associated myelitis, which are useful for differentiating MOGAD from both multiple sclerosis and neuromyelitis optica spectrum disorder. In this review we summarize the clinical and radiographic characteristics of MOG-IgG-associated myelitis with a particular focus on adult patients.
Identifiants
pubmed: 35589317
pii: 18.280
doi: 10.3988/jcn.2022.18.3.280
pmc: PMC9163942
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
280-289Subventions
Organisme : National Research Foundation of Korea
ID : NRF-2018R1A5A2023127
Pays : Korea
Informations de copyright
Copyright © 2022 Korean Neurological Association.
Déclaration de conflit d'intérêts
KH Kim reports no disclosures.
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