A Case of Best Vitelliform Macular Dystrophy

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Identifier 20210220_nanos_posters_064
Title A Case of Best Vitelliform Macular Dystrophy
Creator Michael Vaphiades
Affiliation University of Alabama at Birmingham, Birmingham, AL
Subject Retina; Pediatric Neuro-ophthalmology; Diagnostic Tests (ERG, VER, OCT, HRT, mfERG, etc); Miscellaneous; Genetic Disease
Description Best vitelliform macular dystrophy (BVMD) is the second most common hereditary macular dystrophy. The most common heritable juvenile-onset macular dystrophy is Stargardt disease. BVMD is a rare autosomal dominant disorder manifesting with slow visual loss from retinal degeneration. We present a case of BVMD and review the diagnosis and testing required to make the diagnosis.
Date 2021-02
Language eng
Format application/pdf
Type Text
Source 2021 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS Annual Meeting 2021: Poster Session I: Ocular-Imaging
Collection Neuro-Ophthalmology Virtual Education Library: NANOS Annual Meeting Collection: https://novel.utah.edu/collection/nanos-annual-meeting-collection/
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2021. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6ms9pfj
Setname ehsl_novel_nam
ID 1675769
Reference URL https://collections.lib.utah.edu/ark:/87278/s6ms9pfj
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