Page last updated: 2024-10-20

succinic acid and Ornithine Carbamoyltransferase Deficiency Disease

succinic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 2 studies

Succinic Acid: A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
succinic acid : An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. It is an intermediate metabolite in the citric acid cycle.

Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kodama, H2
Nose, O2
Okada, S2
Maki, I1
Tajiri, H1
Sano, T1
Yabuuchi, H2

Other Studies

2 other studies available for succinic acid and Ornithine Carbamoyltransferase Deficiency Disease

ArticleYear
Organic acid metabolism in a patient with ornithine transcarbamylase deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 1982, Aug-04, Volume: 123, Issue:1-2

    Topics: Ammonia; Ammonium Chloride; Child; Citrates; Citric Acid; Female; Glutamine; Humans; Ketoglutaric Ac

1982
The study of organic acids metabolism in a patient with ornithine transcarbamylase (OTC) deficiency.
    Advances in experimental medicine and biology, 1982, Volume: 153

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Citrates; Citric Acid; Female; Humans; Ketoglu

1982