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Advancing the Understanding of Primary Hyperoxaluria: Insights from Two Compelling Case Reports

Primary hyperoxaluria (PH) encompasses a group of rare genetic disorders marked by the overproduction of oxalate, leading to severe complications such as end-stage renal disease (ESRD). Among the various types, Primary Hyperoxaluria-1 (PH1) and Primary Hyperoxaluria-2 (PH2) stand out, each presenting distinct genetic underpinnings and clinical manifestations. In this article,...