Identifier |
wh_ch46_p2500 |
Title |
Walsh & Hoyt: Disorders of Mitochondria |
Creator |
Michael X. Repka, MD |
Subject |
Neurodegenerative Diseases; Metabolic Diseases; Infant; Child; Mitochondria Disorders |
Description |
The mitochondrial encephalomyopathies are caused by defects in oxidative phosphorylation in mitochondria. Energy-dependent tissues are most vulnerable. These include muscle, brain, retina, and optic nerve. These diseases may be caused by mutations of either the mitochondrial DNA or nuclear DNA. Disorders of ophthalmologic interest include the Kearns-Sayre syndrome, Lebers hereditary optic neuropathy, the syndrome of myoclonic epilepsy and ragged red fibers (MERRF syndrome), the syndrome of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS syndrome), and subacute necrotizing encephalomyelopathy (Leighs disease). |
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/s60c846p |
Setname |
ehsl_novel_whts |
ID |
186154 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s60c846p |