Xq26.3 Microdeletion in a Male with Wildervanck Syndrome

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Identifier 20130212_nanos_posters_127
Title Xq26.3 Microdeletion in a Male with Wildervanck Syndrome
Creator Thomas M. Bosley; Altaf Kondkar; Ibrahim A. Alorainy; Arif O. Khan; Darren T. Oystreck; Khaled K. Abu-Amero
Affiliation (TMB) (AK) (DTO) (KKA) Department of Ophthalmology, King Saud University, Riyadh, Saudi Arabia; (IAA) Department of Radiology, King Saud University, Riyadh, Saudi Arabia; (AOK) Department of Ophthalmology, King Khalid Eye Specialist Hospital, Riyadh, Saudi Arabia
Subject Wildervanck Syndrome; Duane Retraction Syndrome; Medical Genetics; Congenital Eye Movement Abnormality; Congenital Deafness
Description Wildervanck syndrome (cervico-oculo-acoustic syndrome) consists of the Klippel-Feil anomaly, Duane retraction syndrome, and congenital deafness. It is much more common in females than males and could be due to an X-linked mutation that is lethal to hemizygous males. We present the genetic evaluation of a male with Wildervanck syndrome and his family.
Date 2013-02-12
Language eng
Format application/pdf
Type Text
Source 2013 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2013: 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/s6zk8pbv
Setname ehsl_novel_nam
ID 183342
Reference URL https://collections.lib.utah.edu/ark:/87278/s6zk8pbv
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