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 |