Microvascular Changes in Wolfram Syndrome

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Identifier 20200310_nanos_posters_256
Title Microvascular Changes in Wolfram Syndrome
Creator Olinda Faria, Ana Maria Cunha, Sérgio Estrela Silva, Fernando Falcão-Reis
Subject Genetic Disease, Neuro-ophth & Systemic Disease (eg. MS, MG, Thyroid), Optic Neuropathy
Description Wolfram syndrome (WS) is a rare autosomal recessive progressive neurodegenerative disease. The purpose of this work is to evaluate systemic, genetic and ophthalmic characteristics, including optical coherence tomography angiography (OCTA) measurements of capillary network vessel density (VD), in patients with WS.
Relation is Part of NANOS Annual Meeting 2020: Poster Session II: Scientific Advancements
Contributor Primary Olinda Faria
Contributor Secondary Ana Maria Cunha, Sérgio Estrela Silva, Fernando Falcão-Reis
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2020-03
Format application/pdf
Source 2020 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2020. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Language eng
ARK ark:/87278/s6h18bgz
Setname ehsl_novel_nam
Date Created 2020-04-21
Date Modified 2020-05-28
ID 1542123
Reference URL https://collections.lib.utah.edu/ark:/87278/s6h18bgz
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