Page last updated: 2024-10-18

glutaric acid and Embryopathies

glutaric acid has been researched along with Embryopathies in 6 studies

glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.

Research Excerpts

ExcerptRelevanceReference
"When pregnancy is terminated because of enlarged hyperechoic kidneys in the fetus, autopsy is crucial for establishing the correct diagnosis."1.30Recurrent fetal polycystic kidneys associated with glutaric aciduria type II. ( Graem, N; Kjaergaard, S; Larsen, T; Skovby, F, 1998)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's3 (50.00)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hasegawa, Y1
Iga, M1
Kimura, M1
Shigematsu, Y1
Yamaguchi, S1
Hockey, A1
Knowles, S1
Davies, D1
Carey, W1
Hurst, J1
Goldblatt, J1
Kjaergaard, S1
Graem, N1
Larsen, T1
Skovby, F1
Vianey-Saban, C1
Bouvier, R1
Cochat, P1
Buenerd, A1
Divry, P1
Dumoulin, R1
Cordier, MP1
Medlock, MD1
Rhead, WJ1
Pollack, L1
Meredith, JT1
Pearl, G1
Reece, C1
Henderson, HE1
Balla, R1
de Jong, G1
Piek, CJ1
Mienie, LJ1
Erasmus, E1

Other Studies

6 other studies available for glutaric acid and Embryopathies

ArticleYear
Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005, Aug-25, Volume: 823, Issue:1

    Topics: Amniotic Fluid; Carboxylic Acids; Carnitine; Female; Fetal Diseases; Gas Chromatography-Mass Spectro

2005
Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance.
    Birth defects original article series, 1993, Volume: 29, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Female; Fetal Diseases; Genes, Recessive; Gluta

1993
Recurrent fetal polycystic kidneys associated with glutaric aciduria type II.
    APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 1998, Volume: 106, Issue:12

    Topics: Acyl-CoA Dehydrogenases; Adult; Female; Fetal Diseases; Glutarates; Humans; Polycystic Kidney Diseas

1998
Antenatal expression of multiple acyl-CoA dehydrogenase deficiency.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:4

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Cells, Cultured; Electron-Transferring Flavoprotein

2000
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling.
    Journal of perinatology : official journal of the California Perinatal Association, 1991, Volume: 11, Issue:3

    Topics: Acidosis; Cerebral Hemorrhage; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Fetal Di

1991
Postnatal and antenatal laboratory diagnosis of glutaric aciduria II in a South African family.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1987, May-02, Volume: 71, Issue:9

    Topics: Female; Fetal Diseases; Glutarates; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Pregna

1987