The Mitochondrial Myopathy Encephalopathy, Lactic Acidosis with Stroke-Like Episodes (MELAS) SyndromeA Review of Treatment Options

被引：0
|
作者：
Fernando Scaglia
Jennifer L. Northrop
机构：
[1] Baylor College of Medicine and Texas Children’s Hospital,Department of Molecular and Human Genetics
[2] Clinical Care Center,undefined
来源：
CNS Drugs | 2006年 / 20卷
关键词：
Lactic Acidosis; CoQ10; Creatine Supplementation; Idebenone; Leigh Syndrome;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Mitochondrial encephalomyopathies are a multisystemic group of disorders that are characterised by a wide range of biochemical and genetic mitochondrial defects and variable modes of inheritance. Among this group of disorders, the mitochondrial myopathy, encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome is one of the most frequently occurring, maternally inherited mitochondrial disorders.
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页码：443 / 464
页数：21
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