lactic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 2 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
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)
| Excerpt | Relevance | Reference |
|---|---|---|
| "In Europe Reye's syndrome is a rather rare but often fatal disease affecting children and teenagers." | 1.27 | [Reye syndrome--a status review of current concepts of its pathogenesis]. ( Plauth, M, 1984) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Plauth, M | 1 |
| Kodama, H | 1 |
| Nose, O | 1 |
| Okada, S | 1 |
| Yabuuchi, H | 1 |
2 other studies available for lactic acid and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
[Reye syndrome--a status review of current concepts of its pathogenesis].
Topics: Aflatoxins; Ammonia; Aspirin; Carbamoyl-Phosphate Synthase (Ammonia); Child; Fatty Acids, Nonesterif | 1984 |
The study of organic acids metabolism in a patient with ornithine transcarbamylase (OTC) deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Citrates; Citric Acid; Female; Humans; Ketoglu | 1982 |