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glyceric acid and Hyperoxaluria, Primary

glyceric acid has been researched along with Hyperoxaluria, Primary in 9 studies

glyceric acid: found in urine of patient with D-glyceric acidemia & hyperglycinaemia; RN given refers to parent cpd without isomeric designation
glycerol ether : Any ether having glyceryl as at least one of the O-substituents.
glyceric acid : A trionic acid that consists of propionic acid substituted at positions 2 and 3 by hydroxy groups.

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 Excerpts

ExcerptRelevanceReference
"D-glyceric aciduria (DGA) is an autosomal recessive metabolic disorder caused by mutations in the GLYCTK gene."2.61Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review. ( Abu Rashid, M; Elpeleg, O; Eran, A; Jansen, EEW; Mandel, H; Ravid, S; Saada, A; Shaag, A; Spiegel, R; Wamelink, MMC; Zehavi, Y, 2019)
"This may reveal underdiagnosed primary hyperoxaluria, even in older patients."1.46Late diagnosis of primary hyperoxaluria type III. ( Acquaviva, C; Blouin, JM; Bouchet, S; de la Faille, R; Harambat, J; Llanas, B; Richard, E, 2017)
"D-glyceric aciduria is a rare inborn error of serine and fructose metabolism that was first described in 1974."1.36D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK). ( Chang, R; Christensen, E; Fischer, K; Kapelari, K; Sass, JO; Scholl-Bürgi, S; Walter, M; Wang, R, 2010)
"l-Glyceric acid was also isolated from the urine of healthy controls as one of the main peaks."1.33Differential chemical diagnosis of primary hyperoxaluria type II. Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives. ( Inoue, Y; Kuhara, T; Ohse, M; Shinka, T, 2005)
"Type I primary hyperoxaluria (PH I) results from a deficiency of alanine:glyoxylate aminotransferase, whereas type II disease has been traced to a deficiency of D-glycerate dehydrogenase."1.30Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria. ( Dietzen, DJ; Kenagy, DN; Landt, M; Milliner, DS; Smith, CH; Wilhite, TR, 1997)
"Most cases of primary hyperoxaluria are due to deficiency of hepatic peroxisomal alanine:glyoxylate aminotransferase [i."1.29Primary hyperoxaluria type 2. ( Mansell, MA, 1995)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (33.33)18.2507
2000's2 (22.22)29.6817
2010's4 (44.44)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Swanson, MA1
Garcia, SM1
Spector, E1
Kronquist, K1
Creadon-Swindell, G1
Walter, M2
Christensen, E2
Van Hove, JLK1
Sass, JO2
Zehavi, Y1
Mandel, H1
Eran, A1
Ravid, S1
Abu Rashid, M1
Jansen, EEW1
Wamelink, MMC1
Saada, A1
Shaag, A1
Elpeleg, O1
Spiegel, R1
Richard, E1
Blouin, JM1
Harambat, J1
Llanas, B1
Bouchet, S1
Acquaviva, C1
de la Faille, R1
Fischer, K1
Wang, R1
Scholl-Bürgi, S1
Chang, R1
Kapelari, K1
Inoue, Y1
Shinka, T1
Ohse, M1
Kuhara, T1
Rumsby, G1
Mansell, MA1
Dietzen, DJ1
Wilhite, TR1
Kenagy, DN1
Milliner, DS1
Smith, CH1
Landt, M1
Petrarulo, M1
Marangella, M1
Cosseddu, D1
Linari, F1

Reviews

1 review available for glyceric acid and Hyperoxaluria, Primary

ArticleYear
Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review.
    Metabolic brain disease, 2019, Volume: 34, Issue:2

    Topics: Brain Diseases; Child; Epilepsy; Glyceric Acids; Humans; Hyperoxaluria, Primary; Infant; Male; Mutat

2019

Other Studies

8 other studies available for glyceric acid and Hyperoxaluria, Primary

ArticleYear
d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence.
    Molecular genetics and metabolism, 2017, Volume: 121, Issue:2

    Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; Carrier Proteins; Diagnosis, Differential; Epile

2017
Late diagnosis of primary hyperoxaluria type III.
    Annals of clinical biochemistry, 2017, Volume: 54, Issue:3

    Topics: Aged; Carcinoma, Renal Cell; Delayed Diagnosis; Gene Expression; Glyceric Acids; Glycolates; Humans;

2017
D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK).
    Human mutation, 2010, Volume: 31, Issue:12

    Topics: Amino Acid Sequence; Base Sequence; Body Fluids; Child; Child, Preschool; DNA Mutational Analysis; F

2010
Differential chemical diagnosis of primary hyperoxaluria type II. Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005, Aug-25, Volume: 823, Issue:1

    Topics: Diagnosis, Differential; Gas Chromatography-Mass Spectrometry; Glyceric Acids; Humans; Hyperoxaluria

2005
Is liver analysis still required for the diagnosis of primary hyperoxaluria type 2?
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2006, Volume: 21, Issue:8

    Topics: Alcohol Oxidoreductases; Biomarkers; Biopsy; Clinical Enzyme Tests; Glyceric Acids; Hyperoxaluria, P

2006
Primary hyperoxaluria type 2.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 1995, Volume: 10 Suppl 8

    Topics: Adult; Carbohydrate Dehydrogenases; Child, Preschool; Female; Glyceric Acids; Humans; Hyperoxaluria,

1995
Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria.
    Clinical chemistry, 1997, Volume: 43, Issue:8 Pt 1

    Topics: Adolescent; Child; Child, Preschool; Chromatography, Gas; Creatinine; Furans; Glyceric Acids; Glycol

1997
High-performance liquid chromatographic assay for L-glyceric acid in body fluids. Application in primary hyperoxaluria type 2.
    Clinica chimica acta; international journal of clinical chemistry, 1992, Oct-30, Volume: 211, Issue:3

    Topics: Body Fluids; Chromatography, High Pressure Liquid; Glyceric Acids; Humans; Hydrogen-Ion Concentratio

1992