Mitochondrial cytopathy in adults: What we know so far

被引：55

作者：

Cohen, BH ^{[1
]}

Gold, DR ^{[1
]}

机构：

[1] Cleveland Clin Fdn, Dept Neurol, Sect Pediat Neurol, Cleveland, OH 44195 USA

来源：

CLEVELAND CLINIC JOURNAL OF MEDICINE | 2001年 / 68卷 / 07期

关键词：

D O I：

10.3949/ccjm.68.7.625

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Mitochondrial cytopathies are a diverse group of inherited and acquired disorders that result in inadequate energy production. They can be caused by inheritable genetic mutations, acquired somatic mutations, exposure to toxins (including some prescription medications), and the aging process itself. In addition, a number of well-described diseases can decrease mitochondrial energy production; these include hyperthyroidism, hypothyroidism, and hyperlipidemia.

引用

页码：625 / +

页数：20

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