Hidden in CAKUT: Post‐Transplant Diagnosis of Primary Hyperoxaluria Type 1 and Rescue Management Using Lumasiran
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DOI: 10.1111/petr.70079
Abstract: Primary hyperoxaluria type 1 (PH1) is a very rare inherited metabolic disorder characterized by excessive oxalate production due to mutation variants in the alanine‐glyoxylate aminotransferase gene (AGXT). Approximately 4% of PH1 cases are diagnosed after… read more here.
Keywords: post transplant; cakut post; hidden cakut; primary hyperoxaluria ... See more keywords