Clinical Features and Factors Associated With Outcome in Late Adult-Onset Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease

Late adult-onset MOGAD accounts for one-quarter of patients with MOGAD. Optic neuritis is the dominant phenotype in this age group with MOGAD and is under-recognized and frequently misdiagnosed. Outcomes in late adult-onset MOGAD are similar to those in early adult-onset disease.

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Publication Details

Journal
Neurology
Published
2025-05-05
DOI
https://doi.org/10.1212/wnl.0000000000213557
Citations
7
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
10.30
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article

Clinical Features and Factors Associated With Outcome in Late Adult-Onset Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease

Jan-Mendelt Tillema, Laura Cacciaguerra, A. Sebastian López‐Chiriboga, Eoin P. Flanagan et al.
7 citations
Neurology
Multiple Sclerosis Research Studies
10.30
article

Clinical Features and Factors Associated With Outcome in Late Adult-Onset Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease

Jan-Mendelt Tillema, Laura Cacciaguerra, A. Sebastian López‐Chiriboga, Eoin P. Flanagan, Misha Pless, Nisa Vorasoot, Stephanie B. Syc‐Mazurek, Eric Eggenberger, Smathorn Thakolwiboon, Deena Tajfirouz, Cristina Valencia-Sánchez, Nanthaya Tisavipat, Vyanka Redenbaugh, Alessandro Dinoto, Kevin D. Chodnicki, John Jing-Wei Chen, Sean Joseph Pittock, Susan E. Horsman, Kai Guo, Jayawant N. Mandrekar
article en
7 citations

Abstract

Late adult-onset MOGAD accounts for one-quarter of patients with MOGAD. Optic neuritis is the dominant phenotype in this age group with MOGAD and is under-recognized and frequently misdiagnosed. Outcomes in late adult-onset MOGAD are similar to those in early adult-onset disease.

NeurologyVol. 104(10)
University of Verona (IT), Mayo Clinic (US), Khon Kaen University (TH), Jacksonville College (US), Mayo Clinic in Arizona (US), Mayo Clinic in Florida (US)
Good health and well-being
Openalex Percentile: Top 2%
Multiple Sclerosis Research Studies
10.30
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