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Adenine phosphoribosyltransferase deficiency and 2, 8-dihydroxyadenine renal stones: A preventable cause of pediatric renal stones and kidney disease

机译:腺嘌呤磷酸核糖基转移酶缺乏症和2,8-二羟基腺嘌呤肾结石:可预防的小儿肾结石和肾脏疾病

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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.
机译:腺嘌呤磷酸核糖基转移酶缺乏症是从婴儿期到成年晚期的遗传病。常见特征是肾和尿路结石复发和阻塞性症状。石头的特征是射线可透的。 2,黄嘌呤氧化酶阻滞剂别嘌呤醇可阻止8-二羟基腺嘌呤(2,8-DHA)的形成。在这里,我们报道了一个8个月大的女婴,该女婴因结石继发结石而导致阻塞性急性肾脏损伤,并接受了手术切除结石的治疗。结石的分析显示出2、8-DHA晶体。

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