Page last updated: 2024-10-19

phenol and Alkaptonuria

phenol has been researched along with Alkaptonuria in 1 studies

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
BROGREN, N1

Other Studies

1 other study available for phenol and Alkaptonuria

ArticleYear
Case of exogenetic ochronosis from carbolic acid compresses.
    Acta dermato-venereologica, 1952, Volume: 32, Issue:3

    Topics: Alkaptonuria; Humans; Ochronosis; Phenol; Phenols

1952