Literature DB >> 7128645

Renal failure due to 2,8-dihydroxyadenine urolithiasis.

M C Greenwood, M J Dillon, H A Simmonds, T M Barratt, J R Pincott, C Metreweli.   

Abstract

A four-year-old girl presented in renal failure due to dihydroxyadenine urolithiasis. Prior to this she had been fed a high purine macrobiotic diet, rich in pulses and grain. She was comatose, anuric, requiring peritoneal dialysis, and bilateral radiolucent renal calculi were revealed by ultrasonography and retrograde pyelography. 2,8-dihydroxyadenine stones were found at pyelolithotomy, renal biopsy revealed interstitial birefringent crystals, and a complete lack of adenine phosphoribosyl transferase (APRT) was found subsequently in erythrocyte lysates. APRT levels were initially falsely raised due to a blood transfusion on admission. The mother was shown to have heterozygote levels. The child was treated successfully with allopurinol, and a reduction in dietary purine but with only partial return of renal function.

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Year:  1982        PMID: 7128645     DOI: 10.1007/bf00442515

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  15 in total

1.  Adenine intoxication in relation to in vivo formation and deposition of 2,8-dioxyadenine in renal tubules.

Authors:  F S PHILIPS; J B THIERSCH; A BENDICH
Journal:  J Pharmacol Exp Ther       Date:  1952-01       Impact factor: 4.030

2.  The identification of 2,8-dihydroxyadenine, a new component of urinary stones.

Authors:  H A Simmonds; K J Van Acker; J S Cameron; W Snedden
Journal:  Biochem J       Date:  1976-08-01       Impact factor: 3.857

3.  Child's urinary lithiasis revealing a complete deficit in adenine phosphoribosyl transferase.

Authors:  H Debray; P Cartier; A Temstet; J Cendron
Journal:  Pediatr Res       Date:  1976-08       Impact factor: 3.756

4.  Adenine toxicity: a three week intravenous study in dogs.

Authors:  G Lindblad; G Jonsson; J Falk
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1973

5.  [A new metabolic disease: the complete deficit of adenine phosphoribosyltransferase and lithiasis of 2,8-dihydroxyadenine].

Authors:  P Cartier; M Hamet; J Hamburger
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1974-09

6.  [2,8-dihydroxyadenine lithiasis: a new case detected by infra-red analysis].

Authors:  R J Reveillaud; M Daudon; M F Protat; A Vincens; D Graveleau
Journal:  Nouv Presse Med       Date:  1979-10-01

7.  Complete deficiency of adenine phosphoribosyltransferase. Report of a family.

Authors:  K J Van Acker; H A Simmonds; C Potter; J S Cameron
Journal:  N Engl J Med       Date:  1977-07-21       Impact factor: 91.245

8.  Experimental crystal nephropathy (one year study in the pig).

Authors:  D A Farebrother; P Hatfield; H A Simmonds; J S Cameron; A S Jones; A Cadenhead
Journal:  Clin Nephrol       Date:  1975-12       Impact factor: 0.975

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

Authors:  T M Barratt; H A Simmonds; J S Cameron; C F Potter; G A Rose; D G Arkell; D I Williams
Journal:  Arch Dis Child       Date:  1979-01       Impact factor: 3.791

10.  Oxalosis in infancy.

Authors:  M C Morris; T L Chambers; P W Evans; P N Malleson; J R Pincott; G A Rose
Journal:  Arch Dis Child       Date:  1982-03       Impact factor: 3.791

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  16 in total

Review 1.  Evaluation of urinary tract calculi in children.

Authors:  S A Hulton
Journal:  Arch Dis Child       Date:  2001-04       Impact factor: 3.791

2.  Adenine phosphoribosyltransferase deficiency in children.

Authors:  Jérôme Harambat; Guillaume Bollée; Michel Daudon; Irène Ceballos-Picot; Albert Bensman
Journal:  Pediatr Nephrol       Date:  2012-01-03       Impact factor: 3.714

3.  Long-term renal outcomes of APRT deficiency presenting in childhood.

Authors:  Hrafnhildur Linnet Runolfsdottir; Runolfur Palsson; Inger MSch Agustsdottir; Olafur S Indridason; Vidar O Edvardsson
Journal:  Pediatr Nephrol       Date:  2018-11-15       Impact factor: 3.714

4.  Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystals.

Authors:  E Christensen; N J Brandt; T Laxdal
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

Review 5.  Urolithiasis in children: current medical management.

Authors:  J Laufer; H Boichis
Journal:  Pediatr Nephrol       Date:  1989-07       Impact factor: 3.714

6.  Rapid method for the diagnosis of partial adenine phosphoribosyltransferase deficiencies causing 2,8-dihydroxyadenine urolithiasis.

Authors:  F Takeuchi; K Matsuta; T Miyamoto; S Enomoto; S Fujimori; I Akaoka; N Kamatani; K Nishioka
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 7.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

Review 8.  Gout, uric acid and purine metabolism in paediatric nephrology.

Authors:  J S Cameron; F Moro; H A Simmonds
Journal:  Pediatr Nephrol       Date:  1993-02       Impact factor: 3.714

9.  Common characteristics of mutant adenine phosphoribosyltransferases from four separate Japanese families with 2,8-dihydroxyadenine urolithiasis associated with partial enzyme deficiencies.

Authors:  S Fujimori; I Akaoka; K Sakamoto; H Yamanaka; K Nishioka; N Kamatani
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Purine enzyme defects as a cause of acute renal failure in childhood.

Authors:  H A Simmonds; J S Cameron; T M Barratt; M J Dillon; S R Meadow; R S Trompeter
Journal:  Pediatr Nephrol       Date:  1989-10       Impact factor: 3.714

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