A Rare Case of SOX2 Gene Deletion Associated with Bilateral Anophthalmia and Complete Absence of the Visual Pathways and Septum Pellucidum

Update Item Information
Identifier 20140304_nanos_posters_077
Title A Rare Case of SOX2 Gene Deletion Associated with Bilateral Anophthalmia and Complete Absence of the Visual Pathways and Septum Pellucidum
Creator Elmann, Solly; Elmalem, Valerie I
Subject Congenital Bilateral Anophthalmia; Anterior Visual Pathways; Posterior Visual Pathways; Septum Pellucidum
Description We report the initial presentation, evaluation, treatment, and follow up of a rare case of congenital bilateral anophthalmia with complete absence of the anterior and posterior visual pathways and septum pellucidum, associated with deletion of the SOX2 gene.
Date 2014-03-04
Language eng
Format application/pdf
Format Creation application/pdf
Type Text
Source 2014 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2014: Poster Presentations
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights Management Copyright 2013. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s69w3n99
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 184121
Reference URL https://collections.lib.utah.edu/ark:/87278/s69w3n99
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