Myogenic Hyperuricemia
- 9 July 1987
- journal article
- case report
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 317 (2), 75-80
- https://doi.org/10.1056/nejm198707093170203
Abstract
To identify the mechanism of hyperuricemia in glycogen storage diseases (glycogenoses) that affect muscle, we studied the effects of exercise and prolonged rest on purine metabolism in two patients with glycogenosis type III (debrancher deficiency), one patient with type V (muscle phosphorylase deficiency), and one patient with type VII (muscle phosphofructokinase deficiency). All had hyperuricemia except for one patient with glycogenosis type III.Keywords
This publication has 31 references indexed in Scilit:
- Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.JCI Insight, 1985
- Hyperuricemia in glycogen storage disease type I. Contributions by hypoglycemia and hyperglucagonemia to increased urate production.JCI Insight, 1985
- Heterogeneity of the molecular lesions in inherited phosphofructokinase deficiency.JCI Insight, 1983
- Phosphofructokinase (PFK) deficiency due to a catalytically inactive mutant M-type subunitAmerican Journal of Hematology, 1982
- Muscle phosphofructokinase deficiencyNeurology, 1981
- Muscle phosphofructokinase deficiency: Two cases with unusual polysaccharide accumulation and immunologically active enzyme proteinMuscle & Nerve, 1980
- ATP Depletion, a Possible Role in the Pathogenesis of Hyperuricemia in Glycogen Storage Disease Type IJCI Insight, 1978
- The Pathogenesis of Hyperuricemia in Glycogen Storage Disease, Type IPediatric Research, 1977
- Hyponatremia and Vincristine TherapyAmerican Journal of Diseases of Children, 1966
- The interrelationship of glycogen storage disease and goutArthritis & Rheumatism, 1965