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Progressive Demyelination in the Presence of Serum Myelin Oligodendrocyte Glycoprotein-IgG: A Case Report.

Authors :
Gil-Perotin S
Castillo-Villalba J
Carreres-Polo J
Navarré-Gimeno A
Mallada-Frechín J
Pérez-Miralles F
Gascón F
Alcalá-Vicente C
Cubas-Nuñez L
Casanova-Estruch B
Source :
Frontiers in neurology [Front Neurol] 2018 May 15; Vol. 9, pp. 340. Date of Electronic Publication: 2018 May 15 (Print Publication: 2018).
Publication Year :
2018

Abstract

The clinical diagnosis of patients with autoantibodies directed to conformational myelin oligodendrocyte glycoprotein MOG-IgG, can be challenging because of atypical clinical presentation. MOG-IgG seropositivity has been reported in several demyelinating diseases, including relapsing opticospinal syndromes [in the neuromyelitis optica spectrum disorders (NMOSD) and less frequently, in multiple sclerosis (MS)], but it has rarely been associated with the progressive course of disease. To contribute to the characterization of MOG-related demyelination, we describe the case of a patient with progressive demyelinating opticospinal disease, IgG-oligoclonal bands (OCB), and serum MOG-IgG.

Details

Language :
English
ISSN :
1664-2295
Volume :
9
Database :
MEDLINE
Journal :
Frontiers in neurology
Publication Type :
Report
Accession number :
29867746
Full Text :
https://doi.org/10.3389/fneur.2018.00340