glycolytic myopathy

myopathy

[mi-op´ah-the] any disease of a muscle. adj., adj myopath´ic.centronuclear myopathy myotubular myopathy.distal myopathy an autosomal dominant form of muscular dystrophy, appearing in two types. The first has onset in infancy, does not progress past adolescence, and is not incapacitating. The second has onset in adulthood and is called myopathy" >late distal hereditary myopathy. Called also distal muscular dystrophy.glycolytic myopathy any myopathy" >metabolic myopathy resulting from a defect of glycolytic enzyme activity, marked by exercise intolerance and cramping, the accumulation of glycogen in muscle, and recurrent myoglobinuria.late distal hereditary myopathy myopathy" >distal myopathy that sets in usually after age 40, does not affect life span and first affects the small muscles of the hands and feet and then spreads proximally.metabolic myopathy myopathy due to disordered metabolism, usually caused by genetic defects or hormonal dysfunction.mitochondrial myopathy any of a group of myopathies associated with an increased number of enlarged, often abnormal, mitochondria in muscle fibers, manifested by exercise intolerance, generalized weakness, acidosis" >lactic acidosis, infantile tetraparesis, ophthalmoplegia, and cardiac abnormalities.myotubular myopathy a form marked by myofibers resembling the myotubules" >myotubules of early fetal muscle.nemaline myopathy a congenital abnormality of myofibrils in which small threadlike fibers are scattered through the muscle fibers; marked by hypotonia and proximal muscle weakness.ocular myopathy a slowly progressive form affecting the extraocular muscles, with ptosis and progressive immobility of the eyes.

单词	glycolytic myopathy
释义	DictionarySeemyopathyEncyclopediaSeeMyopathy glycolytic myopathy myopathy [mi-op´ah-the] any disease of a muscle. adj., adj myopath´ic.centronuclear myopathy myotubular myopathy.distal myopathy an autosomal dominant form of muscular dystrophy, appearing in two types. The first has onset in infancy, does not progress past adolescence, and is not incapacitating. The second has onset in adulthood and is called myopathy" >late distal hereditary myopathy. Called also distal muscular dystrophy.glycolytic myopathy any myopathy" >metabolic myopathy resulting from a defect of glycolytic enzyme activity, marked by exercise intolerance and cramping, the accumulation of glycogen in muscle, and recurrent myoglobinuria.late distal hereditary myopathy myopathy" >distal myopathy that sets in usually after age 40, does not affect life span and first affects the small muscles of the hands and feet and then spreads proximally.metabolic myopathy myopathy due to disordered metabolism, usually caused by genetic defects or hormonal dysfunction.mitochondrial myopathy any of a group of myopathies associated with an increased number of enlarged, often abnormal, mitochondria in muscle fibers, manifested by exercise intolerance, generalized weakness, acidosis" >lactic acidosis, infantile tetraparesis, ophthalmoplegia, and cardiac abnormalities.myotubular myopathy a form marked by myofibers resembling the myotubules" >myotubules of early fetal muscle.nemaline myopathy a congenital abnormality of myofibrils in which small threadlike fibers are scattered through the muscle fibers; marked by hypotonia and proximal muscle weakness.ocular myopathy a slowly progressive form affecting the extraocular muscles, with ptosis and progressive immobility of the eyes.
随便看	kept me in the picture kept men kept me on kept me on a short leash kept me on a tight leash kept me on ice kept me on my toes kept me on the hop kept me posted kept me quiet kept me up kept me waiting kept mind on kept time kept to kept to herself kept to himself kept to myself kept too many balls in the air kept too many plates spinning kept to oneself kept to ourselves kept to something kept to themselves kept to yourself