Optic neuropathy in Wolfram's syndrome imaged with high-definition spectral domain OCT

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Identifier 20150222_nanos_posters_035
Title Optic neuropathy in Wolfram's syndrome imaged with high-definition spectral domain OCT
Creator Dan Milea; Mani Baskaran; Marion Verschoore; Stéphanie Leruez; Xavier Zanlonghi; Christophe Orssaud; Pascal Reynier; Amati-Bonneau Patrizia; Dominique Bonneau; Christophe Verny; Régis Coutant; Tin Aung; Vincent Procaccio
Affiliation (DM) (MB) (TA) Singapore National Eye Centre, Singapore, Singapore; (DM) (MB) (TA) Singapore Eye Research Institute, Singapore, Singapore; (DM) (TA) Duke_NUS, Singapore, Singapore; (DM) (MV) (SL) (PR) (AP) (DB) (CV) (RC) (VP) Angers University Hospital Angers, France; (XZ) Clinique Sourdille Nantes, France; (CO) HGEP Paris, France
Subject Wolfram Syndrome; Hereditary Optic Neuropathy; Optic Neuropathy; OCT; Genetics
Description Optic neuropathy is a cardinal finding in Wolfram syndrome (WS), which typically also associates at least one of the following findings: diabetes mellitus, diabetes insipidus and deafness. The aim of this study was to describe genetic, clinical and high definition OCT (HD-OCT) findings in patients with an optic neuropathy associated with genetically confirmed Wolfram syndrome.
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/s6c56smh
Setname ehsl_novel_nam
ID 184438
Reference URL https://collections.lib.utah.edu/ark:/87278/s6c56smh
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