Clinical Variability In Wolfram Syndrome: Report of a Sample of 16 Patients (.pdf)

Update item information
Identifier 20160228_nanos_posters_067
Title Clinical Variability In Wolfram Syndrome: Report of a Sample of 16 Patients (.pdf)
Creator Alberto Galvez-Ruiz
Subject Wolfram Syndrome, Congenital Optic Neuropathy, Diabetes Mellitus, Diabetes Insipidus, Hearing Loss
Description Wolfram syndrome is an autosomal recessive disease characterized by the presence of diabetes mellitus (DM), optic atrophy (AO), central diabetes insipidus, hearing loss and neurological disorders such as cerebellar ataxia and psychiatric manifestations. It is caused by mutations in the WFS1 gene. The aim of this study is to present a sample of 16 patients with Wolfram syndrome.
Relation is Part of NANOS Annual Meeting 2016: Poster Presentations
Contributor Primary Alberto Galvez-Ruiz
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2016-02-28
Type Text
Format application/pdf
Format Creation application.pdf
Source 2016 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2016. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Language eng
ARK ark:/87278/s6sv0wp0
Setname ehsl_novel_nam
Date Created 2016-07-21
Date Modified 2016-10-11
ID 185108
Reference URL https://collections.lib.utah.edu/ark:/87278/s6sv0wp0
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