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3-hydroxyisobutyric acid and Hyperoxaluria, Primary

3-hydroxyisobutyric acid has been researched along with Hyperoxaluria, Primary in 1 studies

3-hydroxyisobutyric acid: RN given refers to cpd without isomeric designation
3-hydroxyisobutyric acid : A 4-carbon, branched hydroxy fatty acid and intermediate in the metabolism of valine.

Hyperoxaluria, Primary: A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Konkoľová, J1
Chandoga, J1
Kováčik, J1
Repiský, M1
Kramarová, V1
Paučinová, I1
Böhmer, D1

Other Studies

1 other study available for 3-hydroxyisobutyric acid and Hyperoxaluria, Primary

ArticleYear
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
    BMC medical genetics, 2017, 05-31, Volume: 18, Issue:1

    Topics: Alcohol Oxidoreductases; Aminoisobutyric Acids; DNA Mutational Analysis; Female; Gas Chromatography-

2017