Glicklich D, Gruber H E, Matas A J, Tellis V A, Karwa G, Finley K, Salem C, Soberman R, Seegmiller J E
Department of Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10467.
Q J Med. 1988 Oct;68(258):785-93.
We report a case of homozygous adenine phosphoribosyl transferase (APRT) deficiency associated with 2,8-dihydroxyadenine stones recurrent in a patient with a renal transplant. The disease was diagnosed 23 years after the initial episode of renal colic. At that time the disease was unknown. Our patient is only the second case of this disorder reported from the United States. Correct diagnosis is important because long-term maintenance with allopurinol and a low purine diet can effectively prevent stone formation and renal failure.
我们报告一例肾移植患者发生纯合子腺嘌呤磷酸核糖转移酶(APRT)缺乏症并伴有2,8 - 二羟基腺嘌呤结石复发的病例。该疾病在首次肾绞痛发作23年后才被诊断出来。当时这种疾病还不为人所知。我们的患者是美国报道的该疾病的第二例病例。正确诊断很重要,因为用别嘌呤醇长期维持治疗和低嘌呤饮食可以有效预防结石形成和肾衰竭。