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Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiency.

作者信息

Simmonds H A, Barratt T M, Webster D R, Sahota A, Van Acker K J, Cameron J S, Dillon M

出版信息

Adv Exp Med Biol. 1980;122A:337-41. doi: 10.1007/978-1-4615-9140-5_55.

DOI:10.1007/978-1-4615-9140-5_55
PMID:7424654
Abstract

APRT deficiency may be totally benign or life threatening. The importance of early recognition/diagnosis is thus stressed. Urolithiasis (2,8-DHA stones: the precipitating factor in all cases) is treatable. With early recognition and treatment allopurinol without alkali and a diet low in purine homozygotes have remained clinically and biochemically normal to date. 'Uric acid' stones in children must always be suspect and subjected to sophisticated analysis. Diagnosis from red cell APRT activity may also have its pitfalls.

摘要

相似文献

1
Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiency.
Adv Exp Med Biol. 1980;122A:337-41. doi: 10.1007/978-1-4615-9140-5_55.
2
Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new case.
Adv Exp Med Biol. 1980;122A:343-8. doi: 10.1007/978-1-4615-9140-5_56.
3
Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapy.完全性腺嘌呤磷酸核糖转移酶缺乏症中的嘌呤排泄:饮食及别嘌醇治疗的影响
Adv Exp Med Biol. 1977;76B:304-11. doi: 10.1007/978-1-4684-3285-5_46.
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Adenine phosphoribosyltransferase deficiency: 2,8-dihydroxyadenine urolithiasis in a 48-year-old woman.腺嘌呤磷酸核糖转移酶缺乏症:一名48岁女性患2,8-二羟基腺嘌呤尿路结石
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Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child.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。
Arch Dis Child. 1979 Jan;54(1):25-31. doi: 10.1136/adc.54.1.25.
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2,8-Dihydroxyadenine urolithiasis: report of an adult case in the United States.2,8 - 二羟基腺嘌呤尿石症:美国一例成人病例报告。
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[Uric acid stones in children. Identification and therapy of a newly detected defect of adenine-phosphoribosyltransferase (author's transl)].
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2,8-Dihydroxyadeninuria--or when is a uric acid stone not a uric acid stone?
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2,8-dihydroxyadenine stone in children.
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引用本文的文献

1
Rapid method for the diagnosis of partial adenine phosphoribosyltransferase deficiencies causing 2,8-dihydroxyadenine urolithiasis.
Hum Genet. 1985;71(2):167-70. doi: 10.1007/BF00283376.
2
Common characteristics of mutant adenine phosphoribosyltransferases from four separate Japanese families with 2,8-dihydroxyadenine urolithiasis associated with partial enzyme deficiencies.来自四个不同日本家族的与部分酶缺陷相关的2,8 - 二羟基腺嘌呤尿路结石的突变腺嘌呤磷酸核糖转移酶的共同特征。
Hum Genet. 1985;71(2):171-6. doi: 10.1007/BF00283377.