central core myopathy
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Central core disease — Infobox Disease Name = Central core disease Caption = Histopathologic appearance of typical central core disease: NADH TR, transverse section from the rectus femoris. Marked predominance of dark staining, high oxidative type 1 fibres with cores… … Wikipedia
Central-Core-Myopathie — Klassifikation nach ICD 10 G71.2 Angeborene Myopathien Zentralfibrillenmyopathie (Central Core Krankheit) … Deutsch Wikipedia
Central Core Disease — Klassifikation nach ICD 10 G71.2 Angeborene Myopathien Zentralfibrillenmyopathie (Central Core Krankheit) … Deutsch Wikipedia
central core disease — an autosomal dominant form of myopathy characterized by dense, amorphous hyaline changes in the central portion of the myofibrils, which lack organelles. Onset is in infancy and causes delayed motor development, especially in the lower limbs.… … Medical dictionary
Myopathy — Classification and external resources ICD 10 G71 G72, M60 M … Wikipedia
Congenital myopathy — Classification and external resources ICD 10 G71.2 ICD 9 359.0 … 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
Nemaline myopathy — Classification and external resources ICD 10 G71.2 ICD 9 359.0 … Wikipedia
Inflammatory myopathy — Classification and external resources Micrograph of dermatomyositis, a type of inflammatory myopathy. Muscle biopsy. H E stain … Wikipedia
Mitochondrial myopathy — Classification and external resources Simplified structure of a typical mitochondrion ICD 10 G … Wikipedia
