Literature DB >> 7577413

Acute renal failure due to xanthine stones.

M G Bradbury1, M Henderson, J T Brocklebank, H A Simmonds.   

Abstract

A 9-month-old child with the skeletal abnormalities of Fuhrmann's syndrome presented with acute renal failure secondary to bilateral renal calculi. Hereditary xanthinuria was shown to be the underlying metabolic defect. Treatment with allopurinol was unsuccessful at reducing the xanthine excretion.

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Year:  1995        PMID： 7577413     DOI： 10.1007/BF00866732

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


  7 in total

1.  Hereditary xanthinuria with severe urolithiasis occurring in infancy as renal tubular acidosis and hypercalciuria.

Authors:  R D Fildes
Journal:  J Pediatr       Date:  1989-08       Impact factor: 4.406

2.  Hereditary xanthinuria presenting in infancy with nephrolithiasis.

Authors:  T O Carpenter; R L Lebowitz; D Nelson; S Bauer
Journal:  J Pediatr       Date:  1986-08       Impact factor: 4.406

Review 3.  Xanthine stone formation.

Authors:  J E Seegmiller
Journal:  Am J Med       Date:  1968-11       Impact factor: 4.965

4.  Hereditary xanthinuria: report on three patients and short review of the literature.

Authors:  R A Frayha; I S Salti; A Arnaout; A Khatchadurian; S M Uthman
Journal:  Nephron       Date:  1977       Impact factor: 2.847

5.  Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.

Authors:  S K Wadman; M Duran; F A Beemer; B P Cats; J L Johnson; K V Rajagopalan; J M Saudubray; H Ogier; C Charpentier; R Berger
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

6.  Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndrome.

Authors:  W Fuhrmann; A Fuhrmann-Rieger; F de Sousa
Journal:  Eur J Pediatr       Date:  1980-03       Impact factor: 3.183

7.  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
  7 in total
  11 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.  Xanthinuria type I: a rare cause of urolithiasis.

Authors:  Nina Arikyants; Ashot Sarkissian; Albrecht Hesse; Thomas Eggermann; Ernst Leumann; Beat Steinmann
Journal:  Pediatr Nephrol       Date:  2006-11-09       Impact factor: 3.714

Review 3.  When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indications.

Authors:  H A Simmonds; J A Duley; L D Fairbanks; M B McBride
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

4.  Hereditary xanthinuria and urolithiasis in a domestic shorthair cat.

Authors:  E Furman; E H Hooijberg; E Leidinger; C Zedinger; U Giger; J Leidinger
Journal:  Comp Clin Path       Date:  2015-01-30

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

6.  Modern diagnostic approach to hereditary xanthinuria.

Authors:  Martin Mraz; Olha Hurba; Josef Bartl; Zdenek Dolezel; Anthony Marinaki; Lynette Fairbanks; Blanka Stiburkova
Journal:  Urolithiasis       Date:  2014-11-06       Impact factor: 3.436

7.  Deletion of Mocos Induces Xanthinuria with Obstructive Nephropathy and Major Metabolic Disorders in Mice.

Authors:  Delphine Sedda; Claire Mackowiak; Julie Pailloux; Elodie Culerier; Ana Dudas; Pauline Rontani; Nicolas Erard; Antoine Lefevre; Sylvie Mavel; Patrick Emond; Frederic Foucher; Marc Le Bert; Valerie F J Quesniaux; Michael J Mihatsch; Bernhard Ryffel; Madeleine Erard-Garcia
Journal:  Kidney360       Date:  2021-09-17

8.  Renal stone and chronic kidney failure associated with hypouricemia: Answers.

Authors:  Gulsah Kaya Aksoy; Mustafa Koyun; Kimiyoshi Ichida; Elif Comak; Sema Akman
Journal:  Pediatr Nephrol       Date:  2018-12-19       Impact factor: 3.714

Review 9.  Mechanistic insights into xanthine oxidoreductase from development studies of candidate drugs to treat hyperuricemia and gout.

Authors:  Takeshi Nishino; Ken Okamoto
Journal:  J Biol Inorg Chem       Date:  2014-12-12       Impact factor: 3.358

Review 10.  Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.

Authors:  Kimiyoshi Ichida; Yoshihiro Amaya; Ken Okamoto; Takeshi Nishino
Journal:  Int J Mol Sci       Date:  2012-11-21       Impact factor: 5.923
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