Page last updated: 2024-10-16

butyric acid and Acidemia Propionic

butyric acid has been researched along with Acidemia Propionic in 1 studies

Butyric Acid: A four carbon acid, CH3CH2CH2COOH, with an unpleasant odor that occurs in butter and animal fat as the glycerol ester.
butyrate : A short-chain fatty acid anion that is the conjugate base of butyric acid, obtained by deprotonation of the carboxy group.
butyric acid : A straight-chain saturated fatty acid that is butane in which one of the terminal methyl groups has been oxidised to a carboxy group.

Research Excerpts

ExcerptRelevanceReference
"Propionic Acidemia (PA) is a rare metabolic disorder caused by the defect in enzyme (propionyl-coenzyme A (CoA) carboxylase) leading to the abnormal accumulation of metabolites of branched-chain amino acid catabolism in blood and urine."4.12A Rare Case of Propionic Acidemia in a Six Months Female Child. ( Aamir, M; Bibi, A; Chaudhry, N; Haroon, ZH; Irum, S; Rehman, A, 2022)

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's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Irum, S1
Rehman, A1
Aamir, M1
Haroon, ZH1
Chaudhry, N1
Bibi, A1

Other Studies

1 other study available for butyric acid and Acidemia Propionic

ArticleYear
A Rare Case of Propionic Acidemia in a Six Months Female Child.
    Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2022, Volume: 32, Issue:8

    Topics: Amino Acids, Branched-Chain; Butyric Acid; Citrates; Coenzyme A; Female; Glycine; Humans; Infant; Ke

2022