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[代谢性肌病——概述]

[Metabolic myopathies - an overview].

作者信息

Lammens M, Schoser B

机构信息

Departments of Pathology and Neurology, Radboud University Nijmegen Medical Center, The Netherlands.

出版信息

Pathologe. 2009 Sep;30(5):370-8. doi: 10.1007/s00292-009-1170-z.

Abstract

Metabolic disorders of energy production characterise the group of rare, mainly autosomal recessively inherited metabolic muscular diseases which are often associated with multi-systemic symptoms. In this report, an update on the clinics, pathophysiology, pathomorphology and current treatment options of metabolic myopathies will be given. Beyond classic phenotypes of these disorders, one should be aware of oligosymptomatic patients who can be easily missed. The relevant gene mutations and the pathophysiology and pathomorphology they cause are now known for almost all these metabolic diseases. Establishing the correct diagnosis has become even more important since highly specific therapy options are now available for at least some of these inherited disorders, e.g. enzyme replacement therapy in Pompe disease.

摘要

能量产生的代谢紊乱是一组罕见的、主要为常染色体隐性遗传的代谢性肌肉疾病的特征,这些疾病常伴有多系统症状。在本报告中,将对代谢性肌病的临床、病理生理学、病理形态学及当前治疗选择进行更新。除了这些疾病的经典表型外,还应注意那些症状不明显、容易被漏诊的患者。几乎所有这些代谢性疾病的相关基因突变及其引起的病理生理学和病理形态学现在都已明确。由于现在至少对其中一些遗传性疾病有了高度特异性的治疗选择,如庞贝病的酶替代疗法,因此做出正确诊断变得更加重要。

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