Novel Retinal Observations in Genetically Confirmed Kearns Sayre Syndrome

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Identifier 20150224_nanos_posters_218
Title Novel Retinal Observations in Genetically Confirmed Kearns Sayre Syndrome
Creator Thomas M. Bosley; Darren T. Oystreck; Khaled K. Abu-Amero; Sawsan R. Nowilaty; Emma L. Blakely; Robert Taylor; Igor Kozak
Affiliation (TMB) (KKA) King Saud University/Ophthalmology, Riyadh, Saudi Arabia; (DTO) University of Stellenbosch/Ophthalmology, Tygerberg, South Africa; (SRN) (IK) King Khaled Eye Specialist Hospital/Ophthalmology, Riyadh, Saudi Arabia; (ELB) (RT) Newcastle University/Wellcome Trust Centre for Mitochondrial Research Newcastle Upon Tyne, United Kingdom
Subject Kearns Sayre Syndrome; Mitochondria; Pigmentary Retinopathy; Epiretinal Fibrosis; Progressive External Ophthalmoplegia
Description Kearns Sayre Syndrome (KSS) is a complex mitochondrial syndrome typically caused by a single, large-scale mitochondrial DNA (mtDNA) deletion that presents before the age of 20 years with progressive external ophthalmoplegia, pigmentary retinopathy, and other neurologic and medical problems. We emphasize the retinal changes, including several novel observations, in three clinically and genetically characterized patients with KSS.
Date 2015-02-24
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/s66h7q71
Setname ehsl_novel_nam
ID 184834
Reference URL https://collections.lib.utah.edu/ark:/87278/s66h7q71
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