Renal transplantation in a patient with methylmalonic acidaemia

J Inherit Metab Dis. 1998 Oct;21(7):729-37. doi: 10.1023/a:1005493015489.

Abstract

Renal insufficiency is frequently reported in mutase-deficient methylmalonic acidaemia. We present a case report of a patient with mut- methylmalonic acidaemia who developed chronic tubulointerstitial nephropathy during adolescence. At 24 years of age, she developed end-stage renal failure and underwent renal transplantation. Both plasma and urine methylmalonic acid levels decreased significantly with improved renal function following transplantation. Complications included cyclosporin toxicity and development of diabetes. Renal, metabolic, and clinical status remained improved at 3 years after the kidney transplant.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Amino Acid Metabolism, Inborn Errors / complications*
  • Amino Acid Metabolism, Inborn Errors / physiopathology
  • Female
  • Humans
  • Kidney Failure, Chronic / etiology
  • Kidney Failure, Chronic / surgery*
  • Kidney Transplantation*
  • Methylmalonic Acid / blood
  • Methylmalonic Acid / metabolism*
  • Methylmalonic Acid / urine
  • Methylmalonyl-CoA Mutase / deficiency*
  • Nephritis, Interstitial / etiology
  • Nephritis, Interstitial / therapy

Substances

  • Methylmalonic Acid
  • Methylmalonyl-CoA Mutase