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Saudi J Kidney Dis Transpl ; 30(3): 723-725, 2019.
Article in English | MEDLINE | ID: mdl-31249241

ABSTRACT

Adenine phosphoribosyltransferase deficiency is an inherited condition presenting from infancy to late adulthood. The common features are recurrent kidney and urinary tract stones and obstructive symptoms. The stones are characteristically radiolucent. 2, 8-Dihydroxyadenine (2, 8-DHA) formation is blocked by xanthine oxidase blocker allopurinol. Here, we report the case of an eight-month-old baby girl who presented with obstructive acute kidney injury secondary to calculi which was treated with surgical removal of stone. The analysis of the calculi revealed 2, 8-DHA crystals.


Subject(s)
Acute Kidney Injury/etiology , Adenine Phosphoribosyltransferase/deficiency , Adenine/analogs & derivatives , Kidney Calculi/etiology , Metabolism, Inborn Errors/complications , Urolithiasis/complications , Acute Kidney Injury/diagnosis , Acute Kidney Injury/metabolism , Acute Kidney Injury/surgery , Adenine/metabolism , Allopurinol/therapeutic use , Crystallization , Enzyme Inhibitors/therapeutic use , Female , Humans , Infant , Kidney Calculi/diagnosis , Kidney Calculi/metabolism , Kidney Calculi/surgery , Metabolism, Inborn Errors/diagnosis , Metabolism, Inborn Errors/drug therapy , Treatment Outcome , Urolithiasis/diagnosis , Urolithiasis/drug therapy , Xanthine Oxidase/antagonists & inhibitors , Xanthine Oxidase/metabolism
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