Primary Hyperoxaluria

Combined liver-kidney transplantation shows promise in treating oxalate bone disease in pediatric patients

Combined liver-kidney transplantation (CLKT) and kidney after liver transplantation (KALT) show promise in treating oxalate bone disease in pediatric patients with primary hyperoxaluria type 1 (PH1), according to a study. The study highlights significant improvements in bone health, including the cessation of pathological fractures and moderate catch-up growth, following successful...