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

نویسندگان

  • K Ichida
  • M Yoshida
  • R Sakuma
  • T Hosoya
چکیده

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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منابع مشابه

Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.

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Clinical Science and Molecular Medicine (1974) 47,173-178. VARIATIONS IN ALLOPURINOL METABOLISM BY XANTHINURIC SUBJECTS

1. The metabolism of allopurinol was studied in a newly discovered patient with xanthinuria. 2. No oxipurinol was detectable in the urine during allopurinol administration, in direct contrast to the results in a patient previously studied by one of us. 3. Other equally discrepant effects of allopurinol on urinary purine and pyrimidine excretion in these two cases are compared with those in the ...

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عنوان ژورنال:
  • Internal medicine

دوره 37 1  شماره 

صفحات  -

تاریخ انتشار 1998