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Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?

Neuroretinitis, originally described by Leber at the turn of the 20th century, has long perplexed ophthalmologists due to its multiple recognized causes and often atypical presentation. Optic disk edema and macular star in the affected eye are well-agreed upon findings and are due to increased perme...

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Autores principales: Mizera, Thomas, Prospero-Ponce, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637148/
https://www.ncbi.nlm.nih.gov/pubmed/37942586
http://dx.doi.org/10.1177/23247096231206619
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author Mizera, Thomas
Prospero-Ponce, Claudia
author_facet Mizera, Thomas
Prospero-Ponce, Claudia
author_sort Mizera, Thomas
collection PubMed
description Neuroretinitis, originally described by Leber at the turn of the 20th century, has long perplexed ophthalmologists due to its multiple recognized causes and often atypical presentation. Optic disk edema and macular star in the affected eye are well-agreed upon findings and are due to increased permeability of blood vessels near the optic disk and in the retina at large. It also is universally painless and presents with a relative afferent pupillary defect (RAPD) in the affected eye or eyes. However, depending on the infectious agent, an underlying autoimmune condition, or undefined idiopathic cause, there can be various degrees of vision loss, visual field loss, progression or recurrence, as well as involvement of the other eye. We present this case of presumed sequential idiopathic neuroretinitis with severe vision and visual field loss with a low-positive anti-MOG test in the border county of El Paso.
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spelling pubmed-106371482023-11-11 Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive? Mizera, Thomas Prospero-Ponce, Claudia J Investig Med High Impact Case Rep Case Report Neuroretinitis, originally described by Leber at the turn of the 20th century, has long perplexed ophthalmologists due to its multiple recognized causes and often atypical presentation. Optic disk edema and macular star in the affected eye are well-agreed upon findings and are due to increased permeability of blood vessels near the optic disk and in the retina at large. It also is universally painless and presents with a relative afferent pupillary defect (RAPD) in the affected eye or eyes. However, depending on the infectious agent, an underlying autoimmune condition, or undefined idiopathic cause, there can be various degrees of vision loss, visual field loss, progression or recurrence, as well as involvement of the other eye. We present this case of presumed sequential idiopathic neuroretinitis with severe vision and visual field loss with a low-positive anti-MOG test in the border county of El Paso. SAGE Publications 2023-11-09 /pmc/articles/PMC10637148/ /pubmed/37942586 http://dx.doi.org/10.1177/23247096231206619 Text en © 2023 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Mizera, Thomas
Prospero-Ponce, Claudia
Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title_full Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title_fullStr Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title_full_unstemmed Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title_short Recurrent Idiopathic Neuroretinitis: Anti-MOG Positive?
title_sort recurrent idiopathic neuroretinitis: anti-mog positive?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637148/
https://www.ncbi.nlm.nih.gov/pubmed/37942586
http://dx.doi.org/10.1177/23247096231206619
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