Metabolic Myopathies and the Respiratory System

被引:11
|
作者
Koo, Patrick [1 ]
Sethi, Jigme M. [1 ]
机构
[1] Univ Tennessee, Coll Med Chattanooga, Dept Resp Crit Care & Sleep Med, Erlanger Hlth Syst, 975 East 3rd St,C-735, Chattanooga, TN 37403 USA
关键词
Metabolic myopathies; Glycogen storage disease; Mitochondrial disease; Lipid; Purine; Metabolism; Myopathy; MYOADENYLATE DEAMINASE DEFICIENCY; ENZYME REPLACEMENT THERAPY; GLYCOGEN-STORAGE DISEASES; ACID ALPHA-GLUCOSIDASE; FOREARM EXERCISE TEST; POMPE-DISEASE; MCARDLE-DISEASE; MITOCHONDRIAL MYOPATHIES; INSPIRATORY PRESSURE; VITAL CAPACITY;
D O I
10.1016/j.ccm.2018.02.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Metabolic myopathies are a heterogeneous group of disorders characterized by inherited defects of enzymatic pathways involved in muscle cellular energetics and adenosine triphosphate synthesis. Skeletal and respiratory muscles are the most affected. There are multiple mechanisms of disease. The age of onset and prognosis vary. Metabolic myopathies cause exercise intolerance, myalgia, and an increase in muscle breakdown products during exercise. Some affect smooth muscle such as the diaphragm and cause respiratory failure. The pathophysiology is complex, and the evidence in the literature to guide diagnosis and management is sparse. Treatment is limited. This article discusses the pathophysiology and diagnostic evaluation of these disorders.
引用
收藏
页码:401 / +
页数:11
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