Article: Maladie du spectre des anticorps anti-MOG.
2024 Volume 20, Issue 871, Page(s) 828–832
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 ( ... ...
Title translation | Anti-MOG associated disease. |
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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. |
MeSH term(s) | 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 |
Chemical Substances | Myelin-Oligodendrocyte Glycoprotein ; Autoantibodies |
Language | French |
Publishing date | 2024-04-25 |
Publishing country | Switzerland |
Document type | English Abstract ; Journal Article |
ZDB-ID | 2177010-4 |
ISSN | 1660-9379 |
ISSN | 1660-9379 |
DOI | 10.53738/REVMED.2024.20.871.828 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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