[始于儿童期和青春期的线粒体脑肌病]
[Mitochondrial encephalomyopathies starting in childhood and adolescence].
作者信息
Castro-Gago M, Novo-Rodríguez M I, Eirís-Puñal J
机构信息
Departamento de Pediatría, Hospital General de Galicia, Complejo Hospitalario Universitario de Santiago de Compostela, SERGAS, España.
出版信息
Rev Neurol. 1998 Apr;26 Suppl 1:S61-71.
INTRODUCTION
In this chapter we carry out a review of the current basic clinical and diagnostic aspects of mitochondrial cytopathies due to deficiencies in the mitochondrial respiratory chain complexes, which appear clinically during childhood and/or adolescence.
DEVELOPMENT
The description has been divided into two groups: mitochondrial cytopathies secondary to alterations of the mitochondrial DNA (mtDNA) and mitochondrial cytopathies secondary to alterations of the nuclear DNA (nDNA).
CONCLUSIONS
We conclude by considering the importance of such conditions at this age.
引言
在本章中，我们将对线粒体呼吸链复合物缺乏所致线粒体细胞病的当前基础临床和诊断方面进行综述，这些疾病在儿童期和/或青春期出现临床症状。
进展
描述分为两组：继发于线粒体DNA（mtDNA）改变的线粒体细胞病和继发于核DNA（nDNA）改变的线粒体细胞病。
结论
我们通过考虑这些疾病在这个年龄段的重要性来得出结论。
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