Page last updated: 2024-11-08

aspartic acid and Argininosuccinic Aciduria

aspartic acid has been researched along with Argininosuccinic Aciduria in 2 studies

Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.

Argininosuccinic Aciduria: Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosuccinic acid in body fluids and severe HYPERAMMONEMIA. Clinical features of the neonatal onset of the disorder include poor feeding, vomiting, lethargy, seizures, tachypnea, coma, and death. Later onset results in milder set of clinical features including vomiting, failure to thrive, irritability, behavioral problems, or psychomotor retardation. Mutations in the ARGININOSUCCINATE LYASE gene cause the disorder.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Oberholzer, VG1
Palmer, T1
Iafolla, AK1
Gale, DS1
Roe, CR1

Other Studies

2 other studies available for aspartic acid and Argininosuccinic Aciduria

ArticleYear
Increased excretion of N-carbamoyl compounds in patients with urea cycle defects.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Apr-01, Volume: 68, Issue:1

    Topics: Alanine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Aspartic Acid; Carbamates; Child; Ch

1976
Citrate therapy in argininosuccinate lyase deficiency.
    The Journal of pediatrics, 1990, Volume: 117, Issue:1 Pt 1

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Argininosuccinic Acid; Argininosuccinic Aci

1990