Page last updated: 2024-10-20

purine and Glycogen Storage Disease Type I

purine has been researched along with Glycogen Storage Disease Type I in 3 studies

1H-purine : The 1H-tautomer of purine.
3H-purine : The 3H-tautomer of purine.
9H-purine : The 9H-tautomer of purine.
7H-purine : The 7H-tautomer of purine.

Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.

Research Excerpts

ExcerptRelevanceReference
"Hyperuricemia (serum urate level >7 mg/dL) is caused by accelerated generation of uric acid and/or impaired excretion in the kidney."4.84[Definition and classification of hyperuricemia]. ( Yamamoto, T, 2008)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
HOWELL, RR1
ASHTON, DM1
WYNGAARDEN, JB1
Yamamoto, T1
Nuki, G1

Reviews

2 reviews available for purine and Glycogen Storage Disease Type I

ArticleYear
[Definition and classification of hyperuricemia].
    Nihon rinsho. Japanese journal of clinical medicine, 2008, Volume: 66, Issue:4

    Topics: Alcohol Drinking; Diet, Reducing; Fructose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I;

2008
Human purine metabolism: some recent advances and relationships with immunodeficiency.
    Annals of the rheumatic diseases, 1983, Volume: 42 Suppl 1

    Topics: Adenine Phosphoribosyltransferase; Adenosine Deaminase; Glycogen Storage Disease Type I; Gout; Human

1983

Other Studies

1 other study available for purine and Glycogen Storage Disease Type I

ArticleYear
Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid, and purine abnormalities.
    Pediatrics, 1962, Volume: 29

    Topics: Carbohydrates; Child; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Lip

1962