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3-hydroxykynurenine and Alkaptonuria

3-hydroxykynurenine has been researched along with Alkaptonuria in 1 studies

3-hydroxykynurenine: RN given refers to cpd without isomeric designation
3-hydroxykynurenine : A hydroxykynurenine that is kynurenine substituted by a hydroxy group at position 3.
hydroxykynurenine : A hydroxy-amino acid that is kynurenine substituted by a single hydroxy group at unspecified position. A "closed" class.

Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (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
Jyothy, A1
Reddy, PP1

Other Studies

1 other study available for 3-hydroxykynurenine and Alkaptonuria

ArticleYear
Screening for aminoacid disorders in mental retardation.
    Indian pediatrics, 1984, Volume: 21, Issue:5

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Humans; Infant; Intell

1984