Congenital Processes That Cause Incomitant Strabismus (Video)

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Identifier 20150225_nanos_mechanicalcausesofstrabismus1_04
Title Congenital Processes That Cause Incomitant Strabismus (Video)
Creator Gena Heidary
Subject Congenital Fibrosis of the Extraocular Muscles (CFEOM); Duane Syndrome; Brown Syndrome; Incomitant Strabismus; Congenital Strabismus
Description Congenital cranial dysinnervation disorders or CCDDs comprise a group of complex strabismus disorders that result from aberrant innervation or dysinnervation of extraocular muscles. Historically, many CCDDs were thought to be the result of a primary myopathic process that generated incomitant strabismus. Our current understanding, which has been greatly enhanced by the identification of the genetic basis for many of these conditions, is that the underlying etiology for the CCDDs is a primary disruption of innervation of the extraocular muscles with consequent restrictive strabismus.1-3 The ability to recognize the salient clinical features of the CCDDs is essential for appropriate management both non surgical and surgical, for prognosis, and for work up of associated systemic findings when relevant.
Date 2015-02-26
Language eng
Format video/mp4
Format Creation application/video
Type Image/MovingImage
Source 2015 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS Annual Meeting 2015 Mechanical Causes of Strabismum
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 2015. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s67q258b
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Contributor Primary Gena Heidary
Setname ehsl_novel_nam
ID 184764
Reference URL https://collections.lib.utah.edu/ark:/87278/s67q258b
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