From
Dr. Alexander Bondoc
Primary hyperoxaluria diagnosed after kidney transplant: A review of the literature and case report of aggressive renal replacement therapy and lumasiran to prevent allograft loss
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Read the article on pubmed.ncbi.nlm.nih.gov ↗Article · Oct 2026 · 1 min read
In brief
In brief
This case report describes post-transplant diagnosis of primary hyperoxaluria type 1 and successful allograft preservation using intensive dialysis combined with lumasiran therapy. The article reviews diagnostic challenges when hyperoxaluria presents after kidney transplantation and demonstrates how aggressive renal replacement therapy with targeted RNA interference treatment can prevent graft loss from oxalate deposition.
Written by the GCMD Library team from the article.
Primary hyperoxaluria type 1 is a rare inherited disorder caused by abnormal liver glyoxalate metabolism leading to overproduction of oxalate, progressive kidney disease, and systemic oxalosis. While the disorder typically presents with nephrocalcinosis, recurrent nephrolithiasis, and/or early chron …
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