Mitochondrial encephalomyopathy

Mitochondrial myopathy refers to a group of multi-system diseases that cause abnormalities in the structure and function of mitochondria due to defects in genetic genes, leading to cell respiratory chain and energy metabolism disorders. Those with central nervous system symptoms are called mitochondrial encephalomyopathy. This disease was first detected by Luft in 1962 using modified Gomori Trichrome staining (MGT), and the muscle fibers had ragged red fibers (or ragged red fibers) (Ragged red fiber), and the first case of mitochondrial myopathy was diagnosed. Mitochondrial diseases can also affect the central nervous system at the same time, causing a variety of mitochondrial encephalomyopathy. The disease is a group of clinical syndromes.

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