- Mitochondrial-lipid-glycogen storage myopathy
- 线粒体-脂质-糖原贮积肌病
Medical Chinese dictionary (湘雅医学词典). 2013.
Medical Chinese dictionary (湘雅医学词典). 2013.
Myopathy — Classification and external resources ICD 10 G71 G72, M60 M … 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
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
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
Rhabdomyolysis — Classification and external resources Urine from a person with rhabdomyolysis showing the characteristic brown discoloration as a result of myoglobinuria … Wikipedia
Duchenne muscular dystrophy — Classification and external resources Histopathology of gastrocnemius muscle from patient who died of pseudohypertrophic muscular dystrophy, Duchenne type. Cross section of muscle shows extensive replacement of muscle fibers by adipose cells … Wikipedia
Emery–Dreifuss muscular dystrophy — For other uses of EDMD , see Everybody Draw Mohammed Day. Emery–Dreifuss muscular dystrophy Classification and external resources ICD 10 G71.0 ICD 9 … Wikipedia
Pyruvate dehydrogenase deficiency — Classification and external resources ICD 10 E74.4 ICD 9 271.8 … Wikipedia
Adrenoleukodystrophy — Classification and external resources T2 weighted axial scan at the level of the caudate heads demonstrates marked loss of posterior white matter, with reduced volume and increased signal intensity. The anterior white matter is spared. Features… … Wikipedia
Mohr–Tranebjærg syndrome — Classification and external resources OMIM 304700 Mohr–Tranebjærg syndrome (MTS) is a rare X liked recessive syndrome also known as Deafness dystonia syndrome and caused by mutation in the TIMM8A gene. It was first described in 1960 … Wikipedia