Literature DB >> 17482421

[Recurrent urinary lithiasis revealing hereditary xanthinuria].

Afef Bahlous1, Manef Gasmi, Amira Mohsni, Jaouida Abdelmoula.   

Abstract

INTRODUCTION: Hereditary xanthinuria, due to a purine metabolism disorder, is a rare cause of urinary lithiasis in children. CASE: We report the case of a child aged 3 and a half years, who presented recurrent urinary lithiasis that led to destruction of the right kidney. Infrared spectrophotometric analysis of the calculus concluded that it was composed of 100% xanthine. Laboratory tests showed hypouricemia and hypouricosuria with elevated urinary excretion of oxypurines. These findings led to a diagnosis of hereditary xanthinuria.
CONCLUSION: Early diagnosis of this rare disease is essential to avoid its complications. Metabolic causes must be sought in children with lithiasis.

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Year:  2007        PMID: 17482421     DOI: 10.1016/j.lpm.2007.03.030

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  1 in total

1.  Renal stone and chronic kidney failure associated with hypouricemia: Answers.

Authors:  Gulsah Kaya Aksoy; Mustafa Koyun; Kimiyoshi Ichida; Elif Comak; Sema Akman
Journal:  Pediatr Nephrol       Date:  2018-12-19       Impact factor: 3.714

  1 in total

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