Differential diagnosis of the type of glycogen disease in two adult patients with long history of glycogenosis
| Autor: | F. Huijing, S. Van Creveld |
|---|---|
| Rok vydání: | 1964 |
| Předmět: |
Adult
Blood Glucose medicine.medical_specialty Erythrocytes Phosphorylase Kinase Endocrinology Diabetes and Metabolism Blood lipids Blood sugar Biology Glycerides Glycogen debranching enzyme Diagnosis Differential chemistry.chemical_compound Endocrinology Internal medicine Lactate dehydrogenase Leukocytes medicine Humans Glycogen storage disease Pyruvates Phosphorylase kinase L-Lactate Dehydrogenase Glycogen Histocytochemistry Galactose Glycogen Storage Disease medicine.disease Lipids Liver Glycogen Cholesterol Glucose chemistry Hyperglycemia Lactates Differential diagnosis Blood Chemical Analysis |
| Zdroj: | Metabolism. 13:191-194 |
| ISSN: | 0026-0495 |
| DOI: | 10.1016/0026-0495(64)90132-5 |
| Popis: | A number of determinations, including enzyme determinations in white and red blood cells, have been performed in 2 patients with glycogen storage disease who were described in 1928 and 1932 for the first time. From these tests it is concluded that both patients have a deficiency of debranching enzyme (type III glycogenosis) and not of glucose 6-phosphatase (type I glycogen storage) as was formerly believed. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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