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・ Mitra damasomonteiroi
・ Mitra decurtata
・ Mitra deprofundis
・ Mitra deynzeri
・ Mitra doliolum
・ Mitra dondani
・ Mitra dovpeledi
・ Mitochondrial ferritin
・ Mitochondrial fission
・ Mitochondrial fission factor
・ Mitochondrial fusion
・ Mitochondrial intermediate peptidase
・ Mitochondrial intermembrane space
・ Mitochondrial matrix
・ Mitochondrial membrane transport protein
Mitochondrial myopathy
・ Mitochondrial neurogastrointestinal encephalopathy syndrome
・ Mitochondrial optic neuropathies
・ Mitochondrial permeability transition pore
・ Mitochondrial processing peptidase
・ Mitochondrial protein-transporting ATPase
・ Mitochondrial pyruvate carrier 2
・ Mitochondrial ribosomal death-associated protein 3
・ Mitochondrial ribosomal protein L41
・ Mitochondrial ribosomal protein L42
・ Mitochondrial ROS
・ Mitochondrial shuttle
・ Mitochondrial toxicity
・ Mitochondrial translational release factor 1
・ Mitochondrial trifunctional protein


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Mitochondrial myopathy : ウィキペディア英語版
Mitochondrial myopathy

Mitochondrial myopathies are types of myopathies associated with mitochondrial disease. On biopsy, the muscle tissue of patients with these diseases usually demonstrate "ragged red" muscle fibers. These ragged-red fibers contain mild accumulations of glycogen and neutral lipids, and may show an increased reactivity for succinate dehydrogenase and a decreased reactivity for cytochrome c oxidase. Inheritance is maternal (non-Mendelian extranuclear). There are several subcategories of mitochondrial myopathies.
==Treatment==
Although no cure currently exists, there is hope in treatment for this class of hereditary diseases with the use of an embryotic mitochondrial transplant.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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