Literature DB >> 9510406

Two siblings with classical xanthinuria type 1: significance of allopurinol loading test.

K Ichida1, M Yoshida, R Sakuma, T Hosoya.   

Abstract

Two brothers with classical xanthinuria who lacked xanthine dehydrogenase activity were encountered. Their hypouricemia was caused by underproduction of uric acid. In their duodenal mucosa, no xanthine dehydrogenase (oxidase) activity was detected. The patients had no symptoms except for duodenal ulcer in one case. The conversion of allopurinol to oxipurinol during an allopurinol loading test for determining the type of classical xanthinuria revealed that the patients had classical type 1 xanthinuria, because aldehyde oxidase activity was present. Furthermore, the allopurinol loading test was conducted to determine the optimal examination times and specimens required for this test.

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Year:  1998        PMID: 9510406     DOI: 10.2169/internalmedicine.37.77

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  6 in total

1.  Molybdenum enzymes in higher organisms.

Authors:  Russ Hille; Takeshi Nishino; Florian Bittner
Journal:  Coord Chem Rev       Date:  2011-05-01       Impact factor: 22.315

2.  A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.

Authors:  Akira Iguchi; Takaaki Sato; Mihoko Yamazaki; Kazuyuki Tasaki; Yasushi Suzuki; Noriaki Iino; Hiroshi Hasegawa; Kimiyoshi Ichida; Ichiei Narita
Journal:  CEN Case Rep       Date:  2016-03-03

3.  Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient.

Authors:  Agnieszka Jurecka; Blanka Stiburkova; Jakub Krijt; Wanda Gradowska; Anna Tylki-Szymanska
Journal:  J Inherit Metab Dis       Date:  2010-01-14       Impact factor: 4.982

4.  The renal phenotype of allopurinol-treated HPRT-deficient mouse.

Authors:  Cristina Zennaro; Federica Tonon; Paola Zarattini; Milan Clai; Alessandro Corbelli; Michele Carraro; Marialaura Marchetti; Luca Ronda; Gianluca Paredi; Maria Pia Rastaldi; Riccardo Percudani
Journal:  PLoS One       Date:  2017-03-10       Impact factor: 3.240

Review 5.  Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.

Authors:  Kimiyoshi Ichida; Yoshihiro Amaya; Ken Okamoto; Takeshi Nishino
Journal:  Int J Mol Sci       Date:  2012-11-21       Impact factor: 5.923

Review 6.  Hypouricemia and Urate Transporters.

Authors:  Naoyuki Otani; Motoshi Ouchi; Kazuharu Misawa; Ichiro Hisatome; Naohiko Anzai
Journal:  Biomedicines       Date:  2022-03-11
  6 in total

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