| 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 |