Page last updated: 2024-10-20

uric acid and Adult Fanconi Syndrome

uric acid has been researched along with Adult Fanconi Syndrome in 27 studies

Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.

Research Excerpts

ExcerptRelevanceReference
" On arrival, laboratory test results were significant for hypokalemia, hyperchloremic metabolic acidosis, low uric acid concentration, positive urine anion gap, and proteinuria, which resolved on discontinuation of the drug."7.85Proximal Renal Tubular Acidosis (Fanconi Syndrome) Induced by Apremilast: A Case Report. ( Afridi, F; Kar, P; King-Morris, K; Komarla, A; Perrone, D, 2017)
" On arrival, laboratory test results were significant for hypokalemia, hyperchloremic metabolic acidosis, low uric acid concentration, positive urine anion gap, and proteinuria, which resolved on discontinuation of the drug."3.85Proximal Renal Tubular Acidosis (Fanconi Syndrome) Induced by Apremilast: A Case Report. ( Afridi, F; Kar, P; King-Morris, K; Komarla, A; Perrone, D, 2017)
"A 66-year-old man with kappa-light chain multiple myeloma had adult Fanconi syndrome."1.28Adult Fanconi syndrome secondary to kappa-light chain myeloma: improvement of tubular functions after treatment for myeloma. ( Ando, R; Hamaguchi, H; Kanemitsu, H; Marumo, F; Matsuda, O; Miyake, S; Takemura, T; Uchida, S; Yokota, T, 1990)

Research

Studies (27)

TimeframeStudies, this research(%)All Research%
pre-199019 (70.37)18.7374
1990's2 (7.41)18.2507
2000's3 (11.11)29.6817
2010's3 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Perrone, D1
Afridi, F1
King-Morris, K1
Komarla, A1
Kar, P1
Stiburkova, B1
Sebesta, I1
Du, J1
Jiang, Y1
Wang, O1
Li, M1
Xing, XP1
Xia, W1
Igarashi, T1
Hisatome, I1
Ogino, K1
Igawa, O1
Shigemasa, C1
BEN-ISHAY, D1
DREYFUSS, F1
ULLMANN, TD1
Reem, GH1
Isaacs, M1
Vanamee, P1
Moss, AH1
Gabow, PA1
Kaehny, WD1
Goodman, SI1
Haut, LL1
Moriwaki, Y1
Yamamoto, T1
Takahashi, S1
Hiroishi, K1
Yamakita, J1
Nasako, Y1
Naito, Y1
Higashino, K1
García Nieto, V1
Luis Yanes, MI1
Callejón, A1
Lameire, N1
Mussche, M1
Baele, G1
Kint, J1
Ringoir, S1
Savi, M1
Godin, M1
Bovee, KC1
Joyce, T1
Reynolds, R1
Segal, S1
Diamond, HS2
Meisel, AD2
Dwosh, IL1
Roncari, DA1
Marliss, E1
Fox, IH1
Uchida, S1
Matsuda, O1
Yokota, T1
Takemura, T1
Ando, R1
Kanemitsu, H1
Hamaguchi, H1
Miyake, S1
Marumo, F1
Pronicka, E1
Rowińska, E1
Miłoszewska, E1
Nishida, Y1
Gaspar, GA1
Puig, JG1
Mateos, FA1
Oria, CR1
Gomez, ME1
Gil, AA1
Kramer, HJ1
Gonick, HC1
Vertuno, LL1
Preuss, HG1
Argy, WP1
Schreiner, GE1
Palma-Carlos, AG1
Martins Prata, M1
Gomes d'Oliveira, JJ1
Migueis-Clode, MH1
Kurtzman, NA1
Pillay, VK1
Shirodaria, CV1
Savage, TR1
Gekle, D1
Brunner, H1
Langer, E1

Reviews

3 reviews available for uric acid and Adult Fanconi Syndrome

ArticleYear
[Hypouricemia due to renal tubular dysfunction].
    Nihon rinsho. Japanese journal of clinical medicine, 2003, Volume: 61 Suppl 1

    Topics: Diagnosis, Differential; Fanconi Syndrome; Humans; Kidney Tubules, Proximal; Prognosis; Uric Acid

2003
[Proximal renal tubular dysfunction in insulin-dependent diabetes mellitus].
    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2001, Volume: 21 Suppl 3

    Topics: Calcium; Diabetes Mellitus, Type 1; Fanconi Syndrome; Humans; Kidney Tubules; Magnesium; Uric Acid

2001
[Genetic bases of metabolic tubular nephropathies].
    Minerva medica, 1979, Oct-13, Volume: 70, Issue:44

    Topics: Acidosis, Renal Tubular; Amino Acids; Bartter Syndrome; Cystinuria; Diabetes Insipidus; Fanconi Synd

1979

Other Studies

24 other studies available for uric acid and Adult Fanconi Syndrome

ArticleYear
Proximal Renal Tubular Acidosis (Fanconi Syndrome) Induced by Apremilast: A Case Report.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2017, Volume: 70, Issue:5

    Topics: Acidosis; Acidosis, Renal Tubular; Aged; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Psoriat

2017
Hypouricemia and hyperuricosuria in a pubescent girl: Answers.
    Pediatric nephrology (Berlin, Germany), 2018, Volume: 33, Issue:12

    Topics: Acute Kidney Injury; Allopurinol; Antioxidants; Child; Cystinosis; Diagnosis, Differential; Fanconi

2018
URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient.
    Nephrology (Carlton, Vic.), 2018, Volume: 23, Issue:8

    Topics: Asian People; DNA Mutational Analysis; Fanconi Syndrome; Genetic Predisposition to Disease; Humans;

2018
[Drug-induced hypouricemia: pathophysiology and application to the hyperuricemia with life style related disease].
    Nihon rinsho. Japanese journal of clinical medicine, 2003, Volume: 61 Suppl 1

    Topics: Angiotensin-Converting Enzyme Inhibitors; Anti-Infective Agents; Fanconi Syndrome; Humans; Hyperlipi

2003
Fanconi syndrome with hypouricemia in an adult: family study.
    The American journal of medicine, 1961, Volume: 31

    Topics: Adult; Fanconi Syndrome; Humans; Medical Records; Metabolic Diseases; Uric Acid; Water-Electrolyte I

1961
Renal transport of urate, phosphate and glucose in the Fanconi syndrome.
    The Journal of clinical endocrinology and metabolism, 1967, Volume: 27, Issue:8

    Topics: Absorption; Adult; Biological Transport; Fanconi Syndrome; Female; Glomerular Filtration Rate; Gluco

1967
Fanconi's syndrome and distal renal tubular acidosis after glue sniffing.
    Annals of internal medicine, 1980, Volume: 92, Issue:1

    Topics: Acidosis, Renal Tubular; Adult; Electrolytes; Fanconi Syndrome; Female; Humans; Hydrogen-Ion Concent

1980
Uric acid transport in fanconi syndrome with marked renal hypouricemia: analysis using pyrazinamide and benzbromarone.
    Nephron, 1996, Volume: 74, Issue:2

    Topics: Adolescent; Benzbromarone; Fanconi Syndrome; Humans; Kidney; Male; Pyrazinamide; Time Factors; Uric

1996
Hereditary fructose intolerance: a difficult diagnosis in the adult.
    The American journal of medicine, 1978, Volume: 65, Issue:3

    Topics: Acidosis, Renal Tubular; Adult; Age Factors; Bicarbonates; Carbohydrate Metabolism, Inborn Errors; C

1978
[Hypouricaemia (author's transl)].
    La Nouvelle presse medicale, 1979, Dec-24, Volume: 8, Issue:50

    Topics: Allopurinol; Fanconi Syndrome; Humans; Liver Diseases; Neoplasms; Purine-Pyrimidine Metabolism, Inbo

1979
The fanconi syndrome in Basenji dogs: a new model for renal transport defects.
    Science (New York, N.Y.), 1978, Sep-22, Volume: 201, Issue:4361

    Topics: Amino Acids; Animals; Disease Models, Animal; Dog Diseases; Dogs; Fanconi Syndrome; Female; Glomerul

1978
Renal tubular transport of urate in Fanconi syndrome.
    Advances in experimental medicine and biology, 1977, Volume: 76B

    Topics: Amino Acids; Biological Transport; Fanconi Syndrome; Female; Glomerular Filtration Rate; Glycosuria;

1977
Classification of uricosuric states based upon response to pharmacologic inhibitors of urate transport.
    Advances in experimental medicine and biology, 1977, Volume: 76B

    Topics: Anemia, Sickle Cell; Aspirin; Biological Transport; Diatrizoate; Fanconi Syndrome; Glomerular Filtra

1977
Hypouricemia in disease: a study of different mechanisms.
    The Journal of laboratory and clinical medicine, 1977, Volume: 90, Issue:1

    Topics: Adenocarcinoma; Adult; Aged; Fanconi Syndrome; Fasting; Female; Humans; Hypoparathyroidism; Kidney;

1977
Adult Fanconi syndrome secondary to kappa-light chain myeloma: improvement of tubular functions after treatment for myeloma.
    Nephron, 1990, Volume: 55, Issue:3

    Topics: Aged; Bence Jones Protein; Fanconi Syndrome; Humans; Immunoglobulin kappa-Chains; Kidney Tubules; Ma

1990
Tubular function of kidney after galactose loading in two patients with glycogen storage disease type XL.
    Journal of inherited metabolic disease, 1987, Volume: 10, Issue:3

    Topics: Adolescent; Adult; Bicarbonates; Fanconi Syndrome; Galactose; Galactosemias; Glycogen Storage Diseas

1987
[Hypouricemia].
    Ryumachi. [Rheumatism], 1987, Volume: 27, Issue:4

    Topics: Fanconi Syndrome; Hepatolenticular Degeneration; Humans; Kidney; Purine-Nucleoside Phosphorylase; Pu

1987
Hypouricemia due to renal urate wasting: different types of tubular transport defects.
    Advances in experimental medicine and biology, 1986, Volume: 195 Pt A

    Topics: Adult; Biological Transport; Calcium; Child; Fanconi Syndrome; Female; Hematuria; Humans; Kidney Cal

1986
Effect of maleic acid on sodium-linked tubular transport in experimental Fanconi syndrome.
    Nephron, 1973, Volume: 10, Issue:5

    Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Biological Transport, Active; Calcium; D

1973
Fanconi syndrome following homotransplantation.
    Archives of internal medicine, 1974, Volume: 133, Issue:2

    Topics: Adult; Azathioprine; Cadaver; Carbon Dioxide; Creatinine; Fanconi Syndrome; Glycosuria; Humans; Kidn

1974
[Tubulopathies and amyloid disease: 2 cases of De Toni-Debré-Fanconi syndrome].
    La Nouvelle presse medicale, 1973, Feb-24, Volume: 2, Issue:8

    Topics: Acidosis, Renal Tubular; Amyloidosis; Bicarbonates; Calcium; Fanconi Syndrome; Glycosuria, Renal; Hu

1973
Renal reabsorption of glucose in health and disease.
    Archives of internal medicine, 1973, Volume: 131, Issue:6

    Topics: Biological Transport; Fanconi Syndrome; Female; Glomerular Filtration Rate; Glucose; Glycosuria, Ren

1973
Idiopathic Fanconi syndrome without cystinosis.
    Proceedings of the Royal Society of Medicine, 1969, Volume: 62, Issue:11 Part 1

    Topics: Bone Marrow; Citrates; Cornea; Cystine; Ergocalciferols; Fanconi Syndrome; Female; Glycosuria; Human

1969
[Study of the renal function concerning pathogenesis of de Toni-Debré-Fanconi syndrome].
    Zeitschrift fur Kinderheilkunde, 1970, Volume: 109, Issue:1

    Topics: Aminohippuric Acids; Child; Fanconi Syndrome; Glomerular Filtration Rate; Humans; Kidney Function Te

1970