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 |