gamma-guanidinobutyric acid has been researched along with Hyperargininemia in 1 studies
gamma-guanidinobutyric acid: RN given refers to parent cpd
4-guanidinobutyric acid : A monocarboxylic acid that is butanoic acid substituted by a guanidino group at position 4.
4-guanidinobutanoate : A monocarboxylic acid anion that is the conjugate base of 4-guanidinobutanoic acid.
4-guanidinobutanoic acid : The 4-guanidino derivative of butanoic acid.
Hyperargininemia: A rare autosomal recessive disorder of the urea cycle. It is caused by a deficiency of the hepatic enzyme ARGINASE. Arginine is elevated in the blood and cerebrospinal fluid, and periodic HYPERAMMONEMIA may occur. Disease onset is usually in infancy or early childhood. Clinical manifestations include seizures, microcephaly, progressive mental impairment, hypotonia, ataxia, spastic diplegia, and quadriparesis. (From Hum Genet 1993 Mar;91(1):1-5; Menkes, Textbook of Child Neurology, 5th ed, p51)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| Marescau, B | 1 |
| Lowenthal, A | 1 |
| Terheggen, HG | 1 |
| Esmans, E | 1 |
| Alderweireldt, F | 1 |
1 other study available for gamma-guanidinobutyric acid and Hyperargininemia
| Article | Year |
|---|---|
Guanidino compounds in hyperargininemia.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography, Liquid; Chromatography, Thin Layer; | 1982 |