Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/57700
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dc.contributor.authorMarshall S.-
dc.date.accessioned2026-04-08T22:50:24Z-
dc.date.available2026-04-08T22:50:24Z-
dc.date.copyright2016-
dc.identifier.citationAust Orthopt J. 48, 2016. Date of Publication: 2016.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/57700-
dc.description.abstractAcute macular neuroretinopathy (AMN) is a rare disease of the outer retina, most commonly presenting with a central or paracentral scotoma, wedge-shaped foveal lesions and hyper-reflective lesions, followed by thinning at the inner segment-outer segment junction. Patients report central/ paracentral scotomas which correlate with visual field defects as detected by Amsler grid and automated static visual field testing. The case presented in this paper demonstrates the diagnosis of AMN in the absence of the full range of disease markers and highlights the importance of high density optical coherence tomography scanning in-
dc.publisherOrthoptics Australia-
dc.relation.ispartofAustralian Orthoptic Journal-
dc.subject.meshacute macular neuroretinopathy-
dc.subject.meshspectral domain optical coherence tomography-
dc.subject.meshparacentral lesion-
dc.subject.meshscotoma-
dc.titleA missed case of acute macular neuroretinopathy-
dc.typeArticle-
dc.identifier.affiliationOphthalmology-
dc.publisher.placeAustralia-
dc.identifier.institution(Marshall) Ophthalmology Department, Monash Health, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Marshall) Ophthalmology Department, Monash Health, Melbourne, VIC, Australia-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.cerifentitytypePublications-
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