- respiratory muscle myopathy
- 呼吸肌肌病
Medical Chinese dictionary (湘雅医学词典). 2013.
Medical Chinese dictionary (湘雅医学词典). 2013.
muscle disease — ▪ pathology Introduction any of the diseases and disorders that affect the human muscle system (muscle system, human). Diseases and disorders that result from direct abnormalities of the muscles are called primary muscle diseases; those… … Universalium
Myopathy — Classification and external resources ICD 10 G71 G72, M60 M … Wikipedia
Respiratory disease — Classification and external resources Micrograph of an emphysematous lung; emphysema is a common respiratory disease, strongly associated with smoking. H E stain. ICD … Wikipedia
myopathy — Any abnormal condition or disease of the muscular tissues; commonly designates a disorder involving skeletal muscle. [myo + G. pathos, suffering] carcinomatous m. SYN: Lambert Eaton syndrome. centronuclear m. slowly … Medical dictionary
Nemaline myopathy — Classification and external resources ICD 10 G71.2 ICD 9 359.0 … Wikipedia
Thyrotoxic Myopathy — (TM) is a neuromuscular disorder that develops due to the overproduction of the thyroid hormone thyroxine. Also known as hyperthyroid myopathy, TM is one of many myopathies that lead to muscle weakness and muscle tissue breakdown. Evidence… … Wikipedia
Centronuclear myopathy — Classification and external resources Muscle biopsy from the quadriceps taken at 3 months of age from a girl with X linked centronuclear ( myotubular ) myopathy due to a mutation in the myotubularin (MTM1) gene and extremely skewed X inactivation … Wikipedia
Desmin-related myofibrillar myopathy — Classification and external resources OMIM 601419 Desmin related myofibrillar myopathy is a subgroup of the myofibrillar myopathy diseases and is the result of a mutation in the gene that codes for desmin which prevents it from forming protein… … Wikipedia
nemaline myopathy — a genetically and clinically heterogeneous, mainly congenital myopathy, characterized histologically by the presence of small, rodlike particles in the muscle fibers. Inheritance can be either autosomal dominant or autosomal recessive. The most… … Medical dictionary
Mitochondrial myopathy — A form of muscle disease that leads to progressive muscle weakness. More than 25 types of enzyme abnormalities have been defined that fall into this category. They result in a disease of cell metabolism and are defined by a biopsy of muscle… … Medical dictionary
lipid myopathy — any metabolic myopathy caused by a defect in fatty acid oxidation, with the accumulation of triglycerides in muscle; manifestations depend on the specific enzyme deficiency and include limb and respiratory weakness, cardiomyopathy, encephalopathy … Medical dictionary