Identifier |
20150222_nanos_posters_059 |
Title |
Autosomal Dominant Optic Atrophy In Singapore |
Creator |
Sharon L. Tow; Jing-Liang Loo; P. Amati-Bonneau; D. Bonneau; V. Procaccio; P. Reynier; Dan Milea |
Affiliation |
(SLT) (JLL) (DM) Singapore National Eye, Centre, Singapore, Singapore; (SLT) (JLL) (DM) Singapore Eye Research Institute, Singapore, Singapore; (SLT) (JLL) (DM) Duke-National University of Singapore, Singapore, Singapore; (PAB) (DB) (VP) (DM) Angers University Hospital Angers, France |
Subject |
Genetic Disease; Optic Neuropathy |
Description |
Autosomal dominant optic atrophy (ADOA) is a ubiquitous condition causing bilateral visual loss, most commonly related to mutations in the OPA1 gene, mapped on the chromosome 3q28-q29. Recent data suggests a minimum prevalence of 4.07/100 000 in northern England while ADOA is more rarely reported in Asia. Our study aimed to detect patients with genetically confirmed ADOA in Singapore. |
Date |
2015-02-22 |
Language |
eng |
Format |
application/pdf |
Type |
Text |
Source |
2015 North American Neuro-Ophthalmology Society Annual Meeting |
Relation is Part of |
NANOS 2015: Poster Presentations |
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 2013. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
ARK |
ark:/87278/s6t189fw |
Context URL |
The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/ |
Setname |
ehsl_novel_nam |
ID |
184481 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6t189fw |