Page last updated: 2024-10-18

homogentisic acid and Joint Diseases

homogentisic acid has been researched along with Joint Diseases in 14 studies

Homogentisic Acid: Dihydroxyphenylacetic acid with hydroxyls at the 2 and 5 positions of the phenyl ring.
homogentisic acid : A dihydroxyphenylacetic acid having the two hydroxy substituents at the 2- and 5-positions.

Joint Diseases: Diseases involving the JOINTS.

Research Excerpts

ExcerptRelevanceReference
"Ochronosis is a rare disease caused by an inherited lack of homogentisic acid oxidase."4.79The clinical manifestations of ochronosis: a review. ( De Clerck, LS; Francx, LM; Stevens, WJ; Van Offel, JF, 1995)
"Alkaptonuria is characterized by the accumulation of homogentisic acid (HGA), part of which is excreted in the urine but the excess HGA forms a dark brown ochronotic pigment that deposits in the connective tissue (ochronosis), eventually leading to early-onset severe arthropathy."4.12Alkaptonuria in Russia. ( Kuzin, A; Samarkina, E; Soltysova, A; Zatkova, A, 2022)
"Endogenous ochronosis (EO) or alkaptonuria is an inherited autosomal recessive disease caused by the insufficiency of the enzyme homogentisic acid dioxygenase."3.91Endogenous ochronosis: when clinical suspicion prevails over histopathology. ( García-Briz, MI; Gegúndez-Hernández, H; Mateu-Puchades, A; Moneva-Léniz, LM; Pose-Lapausa, P; Sánchez-Martínez, EM, 2019)
"Alkaptonuria (AKU) is a genetic disorder caused by lack of the enzyme responsible for breaking down homogentisic acid (HGA), an intermediate in tyrosine metabolism."3.77Development of an in vitro model to investigate joint ochronosis in alkaptonuria. ( Davidson, JS; Fraser, WD; Gallagher, JA; Jarvis, JC; Ranganath, LR; Santucci, A; Taylor, AM; Tinti, L; Wilson, PJ; Wlodarski, B, 2011)
"Alkaptonuria (AKU) is an autosomal recessive disorder caused by a deficiency of homogentisate 1,2 dioxygenase (HGD) and characterized by homogentisic aciduria, ochronosis, and ochronotic arthritis."3.77An update on molecular genetics of Alkaptonuria (AKU). ( Zatkova, A, 2011)
" Urine homogentisic acid level was elevated, which is diagnostic for alkaptonuria."3.76Alkaptonuria. ( Anolik, R; Pomeranz, MK; Yancovitz, M, 2010)
"Alkaptonuria is a disease often forgotten because of its rarity."2.82Ochronotic arthropathy in the context of spondyloarthritis differential diagnosis: a case-based review. ( Batalov, A; Batalov, Z; Karalilova, R; Kostova, T, 2022)

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19904 (28.57)18.7374
1990's1 (7.14)18.2507
2000's2 (14.29)29.6817
2010's4 (28.57)24.3611
2020's3 (21.43)2.80

Authors

AuthorsStudies
Soltysova, A1
Kuzin, A1
Samarkina, E1
Zatkova, A2
Kostova, T1
Batalov, Z1
Karalilova, R1
Batalov, A1
Kumps, C1
Stanovici, J1
Chaibi, E1
Campos-Xavier, B1
Pavlidou, DC1
Tran, C1
Sánchez-Martínez, EM1
García-Briz, MI1
Moneva-Léniz, LM1
Gegúndez-Hernández, H1
Pose-Lapausa, P1
Mateu-Puchades, A1
Tinti, L1
Taylor, AM1
Santucci, A1
Wlodarski, B1
Wilson, PJ1
Jarvis, JC1
Fraser, WD1
Davidson, JS1
Ranganath, LR1
Gallagher, JA1
Yancovitz, M1
Anolik, R1
Pomeranz, MK1
Thacker, M1
Garude, S1
Puri, A1
Ogata, J1
Tamura, K1
Miyanishi, K1
Minami, K1
Haranishi, Y1
Tsubaki, T1
Van Offel, JF1
De Clerck, LS1
Francx, LM1
Stevens, WJ1
Friis, J1
Kutty, MK1
Iqbal, QM1
Teh, EC1
Lumpur, K1
Duliapin, VA1
Chepoĭ, VM1

Reviews

3 reviews available for homogentisic acid and Joint Diseases

ArticleYear
Ochronotic arthropathy in the context of spondyloarthritis differential diagnosis: a case-based review.
    Rheumatology international, 2022, Volume: 42, Issue:12

    Topics: Aged; Alkaptonuria; Ascorbic Acid; Cartilage Diseases; Dioxygenases; Homogentisic Acid; Humans; Join

2022
The clinical manifestations of ochronosis: a review.
    Acta clinica Belgica, 1995, Volume: 50, Issue:6

    Topics: Cardiovascular Diseases; Homogentisic Acid; Humans; Joint Diseases; Ochronosis; Pigmentation Disorde

1995
[Ochronotic arthropathy].
    Ugeskrift for laeger, 1973, Dec-03, Volume: 135, Issue:49

    Topics: Alkaptonuria; Ascorbic Acid; Cartilage, Articular; Homogentisic Acid; Humans; Joint Diseases; Ochron

1973

Other Studies

11 other studies available for homogentisic acid and Joint Diseases

ArticleYear
Alkaptonuria in Russia.
    European journal of human genetics : EJHG, 2022, Volume: 30, Issue:2

    Topics: Alkaptonuria; Exons; Homogentisate 1,2-Dioxygenase; Homogentisic Acid; Humans; Joint Diseases; Ochro

2022
Black cartilage: Incidentally discovered articular ochronosis during arthroplasty.
    Journal of inherited metabolic disease, 2021, Volume: 44, Issue:6

    Topics: Alkaptonuria; Arthroplasty, Replacement, Knee; Cartilage; Homogentisic Acid; Humans; Incidental Find

2021
Endogenous ochronosis: when clinical suspicion prevails over histopathology.
    Dermatology online journal, 2019, Apr-15, Volume: 25, Issue:4

    Topics: Alkaptonuria; Female; Homogentisic Acid; Humans; Hyperpigmentation; Joint Diseases; Middle Aged; Och

2019
Development of an in vitro model to investigate joint ochronosis in alkaptonuria.
    Rheumatology (Oxford, England), 2011, Volume: 50, Issue:2

    Topics: Alkaptonuria; Cells, Cultured; Homogentisic Acid; Humans; Joint Diseases; Models, Biological; Ochron

2011
Alkaptonuria.
    Dermatology online journal, 2010, Nov-15, Volume: 16, Issue:11

    Topics: Aged; Alkaptonuria; Arthritis; Cyclohexanones; Female; Homogentisic Acid; Humans; Joint Diseases; Ni

2010
An update on molecular genetics of Alkaptonuria (AKU).
    Journal of inherited metabolic disease, 2011, Volume: 34, Issue:6

    Topics: Alkaptonuria; Chromosome Mapping; Chromosomes, Human, Pair 3; DNA Mutational Analysis; Dominican Rep

2011
Ochronotic arthropathy: arthroscopic findings in the shoulder and the knee.
    Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association, 2003, Volume: 19, Issue:8

    Topics: Adult; Arthroscopy; Cartilage, Articular; Collagen; Collagen Diseases; Homogentisic Acid; Humans; Jo

2003
[Anesthesia in a patient with alkaptonuric ochronosis for total hip arthroplasty].
    Masui. The Japanese journal of anesthesiology, 2008, Volume: 57, Issue:4

    Topics: Aged; Alkaptonuria; Anesthesia, Epidural; Anesthesia, General; Anesthesia, Spinal; Arthroplasty, Rep

2008
Alcaptonuria (Ochronosis).
    JAMA, 1973, Apr-30, Volume: 224, Issue:5 Suppl

    Topics: Alkaptonuria; Homogentisic Acid; Humans; Joint Diseases; Oxygenases; Spinal Diseases

1973
Ochronotic arthropathy: an electron microscopical study with a view on pathogenesis.
    Archives of pathology, 1974, Volume: 98, Issue:1

    Topics: Cartilage, Articular; Cell Nucleus; Cytoplasm; Homogentisic Acid; Humans; Joint Diseases; Knee Joint

1974
[Changes in the synovial membrane and synovial fluid in ochronosis].
    Arkhiv patologii, 1972, Volume: 34, Issue:2

    Topics: Homogentisic Acid; Humans; Joint Diseases; Male; Middle Aged; Ochronosis; Synovial Fluid; Synovial M

1972