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Case Report

Hemodialysis for hyperammonemia associated with ornithine transcarbamylase deficiency

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Pages 1-5 | Published online: 24 Jul 2008

References

  • ChanWKButWMLawCW2002Ammonia detoxification by continuous venovenous haemofiltration in an infant with urea cycle defectHong Kong Med J82071012055368
  • ChangMYFangJTChenY-C1999Continuous venovenous haemofiltration in hyperammonaemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiencyNephrol Dial Transplant141282410344381
  • DavenportAWillEJDavisonAM1990Early changes in intracranial pressure during haemofiltration treatment in patients with grade 4 hepatic encephalopathy and acute oliguric renal failureNephrol Dial Transplant519282113646
  • DonnSMSwartzRDThoeneJG1979Comparison of exchange transfusion, peritoneal dialysis, and hemodialysis for the treatment of hyperammonemia in an anuric newborn infantJ Pediatr956770480015
  • GaspariRArcangeliAMensiS2003Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic comaAnn Emerg Med41104912514690
  • GreeneCLBlitzerMGShapiraE1988Inborn errors of metabolism and Reye syndrome: differential diagnosisJ Pediatr1131 Pt 115693290414
  • HaYMcCannMTTuchmanM1997Substrate-induced conformational change in a trimeric ornithine transcarbamoylaseProc Natl Acad Sci USA94955059275160
  • HawkesNDThomasGAJurewiczA2001Non-hepatic hyperammonaemia: an important, potentially reversible cause of encephalopathyPostgrad Med J777172211677282
  • LeonardJVMcKiernanPJ2004The role of liver transplantation in urea cycle disordersMol Genet Metab81Suppl 1S74815050978
  • LeonardJVMorrisAA2002Urea cycle disordersSemin Neonatol7273512069536
  • MathiasRSKostinerDPackmanS2001Hyperammonemia in urea cycle disorders: role of the nephrologistAm J Kidney Dis3710698011325692
  • MsallMBatshawMLSussR1984Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathiesN Engl J Med310150056717540
  • NassogneMCHéronBTouatiG2005Urea cycle defects: 1 and outcomeJ Inherit Metab Dis284071415868473
  • PetersonDE2003Acute postpartum mental status change and coma caused by previously undiagnosed ornithine transcarbamylase deficiencyObstet Gynecol1025 Pt 212121514607061
  • PiccaSDionisi-ViciCAbeniD2001Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicatorsPediatr Nephrol16862711685590
  • RajpootDKGargusJJ2004Acute hemodialysis for hyperammonemia in small neonatesPediatr Nephrol19390514997371
  • RohininathTCostelloDJLynchT2004Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studiesJ Inherit Metab Dis27285815243986
  • SchaeferFStraubeEOhJ1999Dialysis in neonates with inborn errors of metabolismNephrol Dial Transplant149101810328469
  • SmithWKishnaniPSLeeB2005Urea cycle disorders: clinical presentation outside the newborn periodCrit Care Clin214 SupplS91716227115
  • SummarMLBarrFDawlingS2005Unmasked adult-onset urea cycle disorders in the critical care settingCrit Care Clin214 SupplS1816227111
  • WengTIShihFFChenWJ2004Unusual causes of hyperammonemia in the EDAm J Emerg Med22105715011224
  • WiegandCThompsonTBockGH1980The management of life-threatening hyperammonemia: a comparison of several therapeutic modalitiesJ Pediatr9614247350296
  • WilckenB2004Problems in the management of urea cycle disordersMol Genet Metab81Suppl 1S869115050980
  • YoshinoMSakaguchiYKuriyaN1991A nationwide survey on transient hyperammonemia in newborn infants in Japan: prognosis of life and neurological outcomeNeuropediatrics221982021775216