| 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 |
| Context URL |
The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/ |
| Setname |
ehsl_novel_nam |
| ID |
1675769 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6ms9pfj |
