Literature DB >> 2642113

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

H A Simmonds1, J S Cameron, T M Barratt, M J Dillon, S R Meadow, R S Trompeter.   

Abstract

Acute renal failure (ARF) is not listed as a usual form of presentation in hypoxanthine-guanine phosphoribosyltransferase deficiency, despite the gross uric acid overproduction in the defect. We found that a third of such patients may present in ARF when the urinary uric acid/creatinine ratio may be normal, not raised, and the defect may be suspected from the disproportionate increase in plasma uric acid. This is important in view of the potential confusion of uric acid with 2,8-dihydroxyadenine, the even more insoluble purine excreted in the other salvage enzyme disorder, adenine phosphoribosyltransferase deficiency. In that disorder, presentation in ARF is well recognized, the uric acid/creatinine ratio is also normal, but plasma urate is not raised. Our combined experience in these two disorders underlines the importance of early recognition and treatment with carefully adjusted doses of allopurinol, which may reverse or postpone renal failure.

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Year:  1989        PMID: 2642113     DOI: 10.1007/bf00850222

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  15 in total

1.  Use of intact erythrocytes in the diagnosis of inherited purine and pyrimidine disorders.

Authors:  L D Fairbanks; H A Simmonds; D R Webster
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Problems of diagnosis in an adolescent with hypoxanthine-guanine phosphoribosyltransferase deficiency and acute renal failure.

Authors:  J S Cameron; H A Simmonds; D R Webster; V Wass; A Sahota
Journal:  Adv Exp Med Biol       Date:  1984       Impact factor: 2.622

3.  Hyperuricemia in patients with infectious mononucleosis.

Authors:  J S Dylewski; M Gerson
Journal:  Can Med Assoc J       Date:  1985-05-15       Impact factor: 8.262

4.  Partial deficit of hypoxanthine guanine phosphoribosyl transferase presenting as acute renal failure.

Authors:  A Andrés; M Praga; L M Ruilope; J M Martínez; V G Millet; I Bello; J L Rodicio
Journal:  Nephron       Date:  1987       Impact factor: 2.847

5.  Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies.

Authors:  N Kamatani; C Terai; S Kuroshima; K Nishioka; K Mikanagi
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

6.  Hypoxanthine guanine phosphoribosyl transferase deficiency presenting with gout and renal failure in infancy.

Authors:  P C Holland; M J Dillon; J Pincott; H A Simmonds; T M Barratt
Journal:  Arch Dis Child       Date:  1983-10       Impact factor: 3.791

7.  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

8.  Uric acid crystal-induced nephropathy: evidence for a specific renal lesion in a gouty family.

Authors:  D A Farebrother; J R Pincott; H A Simmons; D J Warren; M J Dillon; J S Cameron
Journal:  J Pathol       Date:  1981-10       Impact factor: 7.996

9.  Renal failure in infancy due to over-production of urate.

Authors:  J A Batch; R P Riek; R B Gordon; J R Burke; B T Emmerson
Journal:  Aust N Z J Med       Date:  1984-12

10.  Renal failure due to 2,8-dihydroxyadenine urolithiasis.

Authors:  M C Greenwood; M J Dillon; H A Simmonds; T M Barratt; J R Pincott; C Metreweli
Journal:  Eur J Pediatr       Date:  1982-07       Impact factor: 3.183

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  10 in total

1.  Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation.

Authors:  Alojz Gregoric; Gwenda M Rabelink; Nadja Kokalj Vokac; Natasa Marcun Varda; Boris Zagradisnik
Journal:  Pediatr Nephrol       Date:  2005-06-18       Impact factor: 3.714

2.  Clinical quiz. Lesch-Nyhan syndrome.

Authors:  M M Bhagat; C J Reid
Journal:  Pediatr Nephrol       Date:  1991-11       Impact factor: 3.714

3.  Acute renal failure due to xanthine stones.

Authors:  M G Bradbury; M Henderson; J T Brocklebank; H A Simmonds
Journal:  Pediatr Nephrol       Date:  1995-08       Impact factor: 3.714

4.  Partial hypoxanthine-guanine phosphoribosyltransferase deficiency presenting as acute renal failure.

Authors:  Sarah Cherian; Charles H Crompton
Journal:  Pediatr Nephrol       Date:  2005-10-21       Impact factor: 3.714

5.  Acute renal failure from xanthine nephropathy during management of acute leukemia.

Authors:  Christopher LaRosa; Laura McMullen; Suzanne Bakdash; Demetrius Ellis; Lakshmanan Krishnamurti; Hsi-Yang Wu; Michael L Moritz
Journal:  Pediatr Nephrol       Date:  2006-10-13       Impact factor: 3.714

Review 6.  When and how does one search for inborn errors of purine and pyrimidine metabolism?

Authors:  H A Simmonds
Journal:  Pharm World Sci       Date:  1994-04-15

Review 7.  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

8.  Lesch-Nyhan syndrome presenting with acute renal failure in a 3-day-old newborn.

Authors:  Ivana Pela; Maria Alice Donati; Elena Procopio; Patrizio Fiorini
Journal:  Pediatr Nephrol       Date:  2007-08-16       Impact factor: 3.714

9.  Partial hypoxanthine-guanine phosphoribosyl transferase deficiency in two Korean siblings--a new mutation.

Authors:  Y Choi; J W Koo; I S Ha; Y Yamada; H Goto; N Ogasawara
Journal:  Pediatr Nephrol       Date:  1993-12       Impact factor: 3.714

10.  Novel HGPRT 293 A>G point mutation presenting as neonatal acute renal failure.

Authors:  Hubert Wong; Janusz Feber; Pranesh Chakraborty; Alfred Drukker; Guido Filler
Journal:  Pediatr Nephrol       Date:  2007-10-13       Impact factor: 3.714

  10 in total

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