Taylor Robert W, Schaefer Andrew M, Barron Martin J, McFarland Robert, Turnbull Douglass M
Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, The Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.
Neuromuscul Disord. 2004 Apr;14(4):237-45. doi: 10.1016/j.nmd.2003.12.004.
Mitochondrial respiratory chain abnormalities are an important cause of neuromuscular disease and may be due to defects of either the mitochondrial or nuclear genome. On account of the clinical and genetic heterogeneity exhibited by the mitochondrial myopathies, their investigation and diagnosis remains a challenge, requiring a combination of techniques including muscle histochemistry, biochemical assessment of respiratory chain function and molecular genetic studies. Here, we describe a step-by-step approach to the clinical and laboratory diagnosis of mitochondrial muscle disease, highlighting the many potential problems that can hinder reaching the correct diagnosis.
线粒体呼吸链异常是神经肌肉疾病的一个重要原因,可能是由于线粒体或核基因组缺陷所致。鉴于线粒体肌病所表现出的临床和遗传异质性,其研究和诊断仍然是一项挑战,需要综合运用包括肌肉组织化学、呼吸链功能的生化评估以及分子遗传学研究等多种技术。在此,我们描述一种线粒体肌肉疾病临床和实验室诊断的逐步方法,强调了许多可能阻碍做出正确诊断的潜在问题。