Identifier |
wh_ch22_p1094 |
Title |
Walsh & Hoyt: Congenital Muscular Dystrophies |
Creator |
Paul H. Phillips, MD |
Affiliation |
University of Arkansas |
Subject |
Ocular Motor System; Extraocular Muscles; Myopathies; Muscular Dystrophy; Ion Channel Disorders; Mitochondrial Myopathies; Encephalomyopathy; Congenital Muscular Dystrophies |
Description |
A number of patients have dystrophic muscle pathology associated with symptoms that are present at birth and a variable clinical course. These patients are said to have congenital muscular dystrophy (CMD). CMD is by no means rare. Rospide et al. believed that it represented 16% of childhood muscular dystrophies, and Donner et al. estimated that it represented 9% of all neuromuscular disorders seen in a pediatric hospital. Fukuyama congenital muscular dystrophy. Muscle-eye-brain disease. Walker-Warburg syndrome. Nosologic relations of congenital muscular dystrophies. |
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/s6xw7t81 |
Setname |
ehsl_novel_whts |
ID |
186077 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6xw7t81 |