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Long-term survival on renal replacement therapy for primary hyperoxaluria type I
P Calzavara1, M Marangella, M Petrarulo
1Transplant Center, General Hospital, Treviso, Italy.
Nephron
|January 1, 1993
Summary
This case study highlights a patient with primary hyperoxaluria type I (PH1) on long-term hemodialysis since 1977. Despite recurrent oxalosis post-transplant, the patient remains active, showcasing PH1 management advancements.
Area of Science:
- Nephrology
- Medical Genetics
- Biochemistry
Background:
- Primary hyperoxaluria type I (PH1) is a rare genetic disorder leading to end-stage renal failure.
- Long-term management and diagnosis in anuric patients present unique challenges.