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线粒体肌病诊断

Mitochondrial myopathy diagnosis.

作者信息

Shoffner J M

机构信息

Molecular Medicine Laboratory, Children's Healthcare of Atlanta, GA 30342, USA.

出版信息

Neurol Clin. 2000 Feb;18(1):105-23. doi: 10.1016/s0733-8619(05)70180-8.

Abstract

Oxidative phosphorylation (OXPHOS) accounts for approximately 95% of the adenosine triphosphate (ATP) produced by the cell. The central nervous system, peripheral nervous system, cardiac muscle, skeletal muscle, and smooth muscle are highly susceptible to dysfunction of this complex enzyme system. Although most OXPHOS diseases are multisystem disorders, the neuromuscular manifestations are often prominent and play an important role in patient diagnosis. To assist the neurologist in evaluating these complex patients, this article focuses on selected samples of OXPHOS diseases with identifiable neuromuscular abnormalities and presents an evaluation algorithm to facilitate patient diagnosis.

摘要

氧化磷酸化(OXPHOS)约占细胞产生的三磷酸腺苷(ATP)的95%。中枢神经系统、外周神经系统、心肌、骨骼肌和平滑肌对这种复杂酶系统的功能障碍高度敏感。虽然大多数氧化磷酸化疾病是多系统疾病,但神经肌肉表现往往很突出,在患者诊断中起重要作用。为帮助神经科医生评估这些复杂的患者,本文重点关注具有可识别神经肌肉异常的氧化磷酸化疾病的特定样本,并提出一种评估算法以促进患者诊断。

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