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• W2130255979 abstract "Adenine phosphoribosyltransferase deficiency is a rare autosomal recessive disorder manifesting as urolithiasis or crystalline nephropathy. It leads to the generation of large amounts of poorly soluble 2,8-dihydroxyadenine excreted in urine, yielding kidney injury and in some patients, kidney failure. Early recognition of the disease, institution of xanthine analog therapy to block the formation of 2,8-dihydroxyadenine, high fluid intake, and low purine diet prevent CKD. Because of symptom variability and lack of awareness, however, the diagnosis is sometimes extremely deferred. We describe a patient with adenine phosphoribosyltransferase deficiency who was diagnosed during evaluation of a poorly functioning second kidney allograft. This report highlights the risk of renal allograft loss in patients with undiagnosed adenine phosphoribosyltransferase deficiency and the need for improved early detection of this disease." @default.
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• W2130255979 date "2014-01-23" @default.
• W2130255979 modified "2023-10-11" @default.
• W2130255979 title "Adenine Phosphoribosyltransferase Deficiency as a Rare Cause of Renal Allograft Dysfunction" @default.
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• W2130255979 doi "https://doi.org/10.1681/asn.2013090960" @default.
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