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propionic acid and Deficiency Disease, Ornithine Carbamoyltransferase

propionic acid has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 3 studies

propionic acid : A short-chain saturated fatty acid comprising ethane attached to the carbon of a carboxy group.

Research Excerpts

ExcerptRelevanceReference
" Seven infants diagnosed with methylmalonyl-CoA mutase deficiency (n=2), ornithine carbamoyltransferase deficiency (n=1), propionic acidaemia (n=1), isovaleric acidaemia (n=1), maple syrup urine disease (n=1) and glutaric acidemia type I (n=1) were tried with breastfeeding over two years."3.73Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. ( Baykal, T; Demir, F; Demirkol, M; Huner, G, 2005)
"Methylmalonic acidemia (MMA) was most common (74 cases), followed by propionic acidemia (23 cases), ornitine transcarbamylase deficiency (22 cases), and multiple carboxylase deficiency (15 cases)."1.33Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening. ( Hasegawa, Y; Hori, D; Kimura, M; Verma, IC; Yamaguchi, S; Yang, Y, 2005)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hori, D1
Hasegawa, Y1
Kimura, M1
Yang, Y1
Verma, IC1
Yamaguchi, S1
Huner, G1
Baykal, T1
Demir, F1
Demirkol, M1
Hyman, SL1
Porter, CA1
Page, TJ1
Iwata, BA1
Kissel, R1
Batshaw, ML1

Other Studies

3 other studies available for propionic acid and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening.
    Brain & development, 2005, Volume: 27, Issue:1

    Topics: Adolescent; Age of Onset; Asia; Carboxylic Acids; Child; Child, Preschool; Disease Progression; Drug

2005
Breastfeeding experience in inborn errors of metabolism other than phenylketonuria.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Breast Feeding; Child, Preschool; Follow-Up Studies; Glutarate

2005
Behavior management of feeding disturbances in urea cycle and organic acid disorders.
    The Journal of pediatrics, 1987, Volume: 111, Issue:4

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Anorexia; Argininosuccinic Acid; Behavior Therapy; Chil

1987