Bone health in children with primary hyperoxaluria type 1 following liver and kidney transplantation
BackgroundPrimary hyperoxaluria type 1 is characterized by hepatic oxalate overproduction, leading to nephrocalcinosis, kidney stones, kidney failure and systemic oxalosis, including oxalate osteopathy. Combined liver-kidney transplantation (CLKT) and kidney after liver transplantation (KALT) were e...
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Frontiers Media S.A.,
2024-02-01T00:00:00Z.
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A1234.567 |
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