Autosomal Dominant Optic Atrophy In Singapore

Update Item Information
Identifier 20150224_nanos_posters_059
Title Autosomal Dominant Optic Atrophy In Singapore
Creator Sharon L. Tow; Jingliang Loo; Patrizia Amati+AC0-Bonneau; Dominique Bonneau; Vincent Procaccio; Pascal 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) (PR) (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
Language eng
Format application/pdf
Type Text
Source 2015 North American Neuro-Ophthalmology Society Annual Meeting
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 2015. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s68m0gzj
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 184787
Reference URL https://collections.lib.utah.edu/ark:/87278/s68m0gzj
Back to Search Results