Background And Purpose: Antibodies to myelin oligodendrocyte glycoprotein (MOG) have been identified in both children and adults with demyelination, with a strong association with bilateral or recurrent optic neuritis (ON). However, the full clinical spectrum of this newly described condition is unknown. We sought to describe non-ON inflammatory ophthalmological presentations such as uveitis and optic perineuritis in the context of MOG antibody seropositivity.
Methods: Using a live cell-based assay analysed by flow cytometry, we identified seropositive patients referred for MOG antibody testing in Australasia between 2014 and 2017. We identified four MOG antibody-positive patients with non-ON inflammatory ophthalmological presentations and present their detailed clinical information in this case series.
Results: Three patients had uveitis either in association with, or remote from, ON. One patient had optic perineuritis and peripheral ulcerative keratitis. We describe the presentation, examination, investigation findings and clinical course of these four patients.
Conclusions: Recognition of these novel clinical associations may expand the clinical spectrum of MOG antibody-associated presentations. An expedited diagnosis may guide the management of these complex patients.
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http://dx.doi.org/10.1111/ene.13932 | DOI Listing |
Ophthalmology
December 2024
Johns Hopkins Medicine, Department of Neurology, Baltimore, Maryland.
Cureus
September 2024
Multiple Sclerosis and Demyelinating Diseases Unit and Center of Expertise for Rare Demyelinating and Autoimmune Diseases of the Central Nervous System, 1st Department of Neurology, "Aeginition" University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, GRC.
A unique case of a female adolescent diagnosed with myelin oligodendrocyte glycoprotein (MOG) monophasic optic neuritis with Epstein-Barr virus (EBV) reactivation antibody profile on a remote Greek island is presented, highlighting the challenges of diagnosing rare conditions in rural settings and the importance of connecting centers of expertise with regional hospitals. The 16-year-old patient presented with progressive vision loss, headache, and retrobulbar pain in the right eye. Initial ophthalmological examinations showed decreased visual acuity and color vision deterioration.
View Article and Find Full Text PDFNeurology
August 2024
From the Departments of Neurology (A.T., K.E.G.) and Pathology (A.W., C.G.E.), Johns Hopkins University, Baltimore, MD.
J Neuroophthalmol
July 2024
Department of Neurology (BP-S), Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan; Departments of Ophthalmology (Y-HL) and Neurology (A-CC), Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; and Departments of Ophthalmology (Y-HL) and Neurology (A-CC), School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
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