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Recurrence of nephrocalcinosis after renal transplantation in an adult patient with primary hyperoxaluria type I.

Abstract
The medical history of a 42-year-old patient with primary hyperoxaluria type I is presented. Primary hyperoxaluria was suspected after renal transplantation, when oxalate deposits were found in a biopsy of the kidney graft. Diagnosis of type I hyperoxaluria was confirmed by the finding that significantly increased amounts of glycolic acid and oxalic acid were excreted. Treatment of the patient with 500 mg pyridoxine daily resulted in a decrease of the excretion of oxalate to normal values.
AuthorsG Knols, K M Leunissen, L J Spaapen, F T Bosman, T W vd Wiel, G Kootstra, J P van Hooff
JournalNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association (Nephrol Dial Transplant) Vol. 4 Issue 2 Pg. 137-9 ( 1989) ISSN: 0931-0509 [Print] England
PMID2496356 (Publication Type: Case Reports, Journal Article)
Topics
  • Adult
  • Female
  • Graft Survival
  • Humans
  • Hyperoxaluria (complications)
  • Hyperoxaluria, Primary (complications, pathology)
  • Kidney (pathology)
  • Kidney Transplantation
  • Kidney Tubules (pathology)
  • Nephrocalcinosis (etiology, pathology)
  • Recurrence

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