hydroxyindoleacetic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 2 studies
(5-hydroxyindol-3-yl)acetic acid : A member of the class of indole-3-acetic acids that is indole-3-acetic acid substituted by a hydroxy group at C-5.
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)
| 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 |
|---|---|
| Bachmann, C | 1 |
| Colombo, JP | 1 |
| Hyman, SL | 1 |
| Porter, CA | 1 |
| Page, TJ | 1 |
| Iwata, BA | 1 |
| Kissel, R | 1 |
| Batshaw, ML | 1 |
2 other studies available for hydroxyindoleacetic acid and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Increase of tryptophan and 5-hydroxyindole acetic acid in the brain of ornithine carbamoyltransferase deficient sparse-fur mice.
Topics: Animals; Brain Chemistry; Carbamoyl-Phosphate Synthase (Ammonia); Female; Hydroxyindoleacetic Acid; | 1984 |
Behavior management of feeding disturbances in urea cycle and organic acid disorders.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Anorexia; Argininosuccinic Acid; Behavior Therapy; Chil | 1987 |