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腺嘌呤磷酸核糖转移酶完全缺乏:一名幼儿出现肾结石的第三例病例。

Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child.

作者信息

Barratt T M, Simmonds H A, Cameron J S, Potter C F, Rose G A, Arkell D G, Williams D I

出版信息

Arch Dis Child. 1979 Jan;54(1):25-31. doi: 10.1136/adc.54.1.25.

Abstract

We report a third case of 2, 8-dihydroxyadenine stones in a child with a complete lack of the adenine salvage enzyme--adenine phosphoribosyltransferase (APRT). The propositus, a 20-month-old girl of consanguineous Arab parents, presented with multiple urinary tract infections and supposed 'uric acid' stones in the right renal pelvis and left ureter. Both parents and one brother were heterzygotes for the defect, in keeping with an autosomal recessive mode of inheritance. In contrast with the other purine salvage enzyme disorder of childhood with true uric acid stones (the Lesch-Nyhan syndrome), uric acid excretion was normal in all family members. As in our previous case, treatment with allopurinol, without alkali, has eliminated the urinary excretion of 2, 8-dihydroxyadenine: the stones were removed surgically. 2, 8-Dihydroxyadenine should be considered in any child thought to have uric acid stones and tests made to distinguish the two compounds.

摘要

我们报告了第三例患有腺嘌呤补救酶——腺嘌呤磷酸核糖转移酶(APRT)完全缺乏的儿童2,8 - 二羟基腺嘌呤结石病例。该患者是一名20个月大的女孩,其父母为近亲结婚的阿拉伯人,因右侧肾盂和左侧输尿管多发尿路感染及疑似“尿酸”结石前来就诊。父母及一个兄弟均为该缺陷的杂合子,符合常染色体隐性遗传模式。与儿童期另一种伴有真性尿酸结石的嘌呤补救酶紊乱疾病(莱施 - 奈恩综合征)不同,所有家庭成员的尿酸排泄均正常。如同我们之前的病例,使用别嘌呤醇且不使用碱进行治疗,已消除了2,8 - 二羟基腺嘌呤的尿排泄:结石通过手术取出。对于任何被认为患有尿酸结石的儿童,都应考虑到2,8 - 二羟基腺嘌呤,并进行检测以区分这两种化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50b5/1545198/f52f7da3c9af/archdisch00797-0033-a.jpg

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