1. Glycogen storage disease, types I to XCriteria for morphologic diagnosis
- Author
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G Hug, Kevin E. Bove, and A J McAdams
- Subjects
Cytoplasm ,Pathology ,medicine.medical_specialty ,Biopsy ,Amylopectin ,Presumptive diagnosis ,Blood sugar ,Glycogen Storage Disease Type I ,Biology ,Glucagon ,Pathology and Forensic Medicine ,Muscular Diseases ,medicine ,Humans ,Glycogen storage disease ,Child ,Electron microscopic ,Cell Nucleus ,medicine.diagnostic_test ,Liver Diseases ,Muscles ,Infant ,Skeletal muscle ,Syndrome ,Glycogen Storage Disease ,medicine.disease ,Microscopy, Electron ,medicine.anatomical_structure ,Liver ,Glucosyltransferases ,Child, Preschool ,Female ,Morphologic diagnosis ,Cardiomyopathies ,Glucosidases ,Hepatomegaly - Abstract
The morphologic features of glycogenosis types I to X are described using light and electron microscopic techniques. With knowledge of the clinical presentation, the effect of intravenously administered glucagon on the blood sugar level, and the morphologic alteration of tissues obtained from liver and skeletal muscle, a presumptive diagnosis can be made in all the glycogenoses. The procedure for definitive diagnosis in each of the glycogenoses is indicated.
- Published
- 1974
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