A Chronic Progressive Optic Neuropathy in a Patient with Anti-Myelin-Oligodendrocyte Glycoprotein (MOG) Antibodies

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Identifier 20190317_nanos_posters_076
Title A Chronic Progressive Optic Neuropathy in a Patient with Anti-Myelin-Oligodendrocyte Glycoprotein (MOG) Antibodies
Creator Doria M. Gold, Laura Balcer, Steven Galetta
Subject Neuro-Ophth & Systyemic Disease (eg. MS, MG, Thyroid); Optic Neuropathy
Description Anti-MOG antibodies have been described in idiopathic inflammatory optic neuritis, such as aquaporin4-IgG seronegative neuromyelitis optica spectrum disorders and chronic relapsing inflammatory optic neuropathy, among others. Visual symptoms are typically characterized by acute onset vision loss and pain with monophasic or relapsing courses. Some cases of optic neuritis are associated with acute disseminated encephalomyelitis or follow it years later. We present a patient with progressive optic neuropathy and anti-MOG antibodies.
Relation is Part of NAM 2019: Poster Session I: Clinical Highlights in Neuro-Ophthalmology
Contributor Primary Doria M. Gold
Contributor Secondary Laura Balcer, Steven Galetta
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2019-03
Format application/pdf
Source 2019 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2019. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Language eng
ARK ark:/87278/s6zs7dxv
Setname ehsl_novel_nam
Date Created 2019-07-18
Date Modified 2019-07-18
ID 1432296
Reference URL https://collections.lib.utah.edu/ark:/87278/s6zs7dxv
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