Walsh & Hoyt: Motility Disorders: Congenital

Identifier wh_ch20_p969
Title Walsh & Hoyt: Motility Disorders: Congenital
Creator Jane C. Sargent, MD
Affiliation Neurology, Clinical Neurophysiology, University of Massachusetts
Subject Ocular Motor System; Ocular Motility Disorders; Congenital Fibrosis; Congenital Adduction Palsy; Vertical Retraction Syndrome; Oculomotor Paresis; Subnuclear
Description Congenital oculomotor nerve palsies are rarer than acquired palsies, but they constitute nearly half of the oculomotor nerve pareses seen in children. Most cases are unilateral, but bilateral cases also occur. As a general rule, patients with congenital oculomotor nerve palsy have no other neurologic or systemic abnormalities, but there are many reports of associated problems such as additional cranial nerve dysfunction, developmental delay, asymmetric hypoplasia of the midbrain and corpus callosum, septo-optic dysplasia, and cerebral palsy. Most cases are sporadic, although rare familial cases occur.
Date 2005
Language eng
Format application/pdf
Type Text
Source Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition
Relation is Part of Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology
Collection Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s66b0c3q
Setname ehsl_novel_whts
ID 186671
Reference URL https://collections.lib.utah.edu/ark:/87278/s66b0c3q