Walsh & Hoyt: Congenital Muscular Dystrophies

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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: NOVEL http://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
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
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