Maladie du spectre des anticorps anti-MOG [Anti-MOG associated disease]

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State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_F1DE110FEDE8
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Maladie du spectre des anticorps anti-MOG [Anti-MOG associated disease]
Journal
Revue medicale suisse
Author(s)
Lerusse J., Uginet M., Théaudin M., Bernard-Valnet R., Pot C., Lalive P.H.
ISSN
1660-9379 (Print)
ISSN-L
1660-9379
Publication state
Published
Issued date
24/04/2024
Peer-reviewed
Oui
Volume
20
Number
871
Pages
828-832
Language
french
Notes
Publication types: English Abstract ; Journal Article
Publication Status: ppublish
Abstract
Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease (MOGAD) is an autoimmune disease responsible for demyelination of the central nervous system that can occur in adults or children. Overlapping phenotypes between MOGAD, multiple sclerosis (MS) and neuromyelitis optica spectrum disease (NMOSD) have been described. The diagnostic criteria for MOGAD were proposed by a panel of international experts and published in 2023. Defining clinical, biological and imaging characteristics specific to this entity helps to improve diagnostic specificity. In this article, we present the clinical characteristics suggestive of MOGAD and discuss the importance of the antibody detection method and therapeutic management.
Keywords
Humans, Myelin-Oligodendrocyte Glycoprotein/immunology, Neuromyelitis Optica/diagnosis, Neuromyelitis Optica/immunology, Autoantibodies/immunology, Autoantibodies/blood, Multiple Sclerosis/diagnosis, Multiple Sclerosis/immunology, Adult, Child, Autoimmune Diseases/diagnosis, Autoimmune Diseases/immunology
Pubmed
Create date
03/05/2024 14:24
Last modification date
04/05/2024 7:20
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