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

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.

[1]  D. Perrett,et al.  Adenine and adenosine metabolism in intact erythrocytes deficient in adenosine monophosphate-pyrophosphate phosphoribosyltransferase: a study of two families. , 1978, Clinical science and molecular medicine.

[2]  G. Panayi,et al.  Functional assay of cytotoxic lymphocytes involved in antibody-mediated cytotoxicity in normal and rheumatoid subjects. , 1977, Annals of the rheumatic diseases.

[3]  B. Emmerson,et al.  Incidence of APRT deficiency. , 1977, Advances in experimental medicine and biology.

[4]  I. Fox Purine enzyme abnormalities: a four year experience. , 1977, Advances in experimental medicine and biology.

[5]  H. Simmonds,et al.  Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapy. , 1977, Advances in experimental medicine and biology.

[6]  G. A. Rose,et al.  The thermogravimetric analysis of renal stones (in clinical practice). , 1976, British journal of urology.

[7]  H. Simmonds,et al.  The identification of 2,8-dihydroxyadenine, a new component of urinary stones. , 1976, The Biochemical journal.

[8]  P. Cartier,et al.  Child's Urinary Lithiasis Revealing a Complete Deficit in Adenine Phosphoribosyl Transferase , 1976, Pediatric Research.

[9]  H. Simmonds,et al.  A New Cause of Urinary Calculi: 2,8-Dihydroxyadenine Stones in Supposed ‘Uric Acid’ Crystalluria , 1976 .

[10]  B. Emmerson,et al.  Adenine phosphoribosyltransferase deficiency: its inheritance and occurrence in a female with gout and renal disease. , 1975, Australian and New Zealand journal of medicine.

[11]  A. De vries,et al.  Recent data on uric acid lithiasis. , 1974, Advances in nephrology from the Necker Hospital.

[12]  B. Emmerson,et al.  Adenine phosphoribosyltransferase deficiency in a female with gout. , 1973, Advances in experimental medicine and biology.

[13]  E. J. Westbury,et al.  A quantitative approach to the analysis of renal calculi. , 1970, The Journal of medical laboratory technology.

[14]  H. Simmonds Urinary excretion of purines, pyrimidines and pyrazolopyrimidines in patients treated with allopurinol or oxipurinol. , 1969, Clinica chimica acta; international journal of clinical chemistry.

[15]  R. Levy,et al.  Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man. , 1968, The Journal of clinical investigation.

[16]  P. Cartier,et al.  Les activités purine-phosphoribosyl transférasiques des globules rouges humains technique de dosage , 1968 .

[17]  C. Dent,et al.  Xanthinuria, an inborn error (or deviation) of metabolism. , 1954, Lancet.

[18]  G. B. Brown,et al.  THE DIRECT OXIDATION OF ADENINE IN VIVO , 1950 .