
Mitochondrial myopathies are characterized by structural and functional abnormalities of the mitochondria. The diseases are best classified according to the underlying biochemical defect. In this article the variability of clinical expression and mitochondrial abnormalities is illustrated. An exact diagnosis is a prerequisite for a rational therapy and genetic counseling. In exceptional cases antenatal diagnosis should be possible.
Muscular Diseases, Histocytochemistry, Infant, Newborn, Cytochrome-c Oxidase Deficiency, Humans, Metabolism, Inborn Errors, Genes, Dominant, Mitochondria, Muscle
Muscular Diseases, Histocytochemistry, Infant, Newborn, Cytochrome-c Oxidase Deficiency, Humans, Metabolism, Inborn Errors, Genes, Dominant, Mitochondria, Muscle
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
