Walsh & Hoyt: Congenital Muscular Dystrophies

Update Item Information
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