Oxalosis (Primary Hyperoxaluria)

  • Gagnadoux M
  • Broyer M
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Abstract

Oxalosis is the systemic deposition of calcium oxalate crystals, caused by primary hyperoxaluria type I (PH I), an autosomal recessive peroxisomal defect involving glyoxylate metabolism in the liver and leading to an excesssive synthesis of oxalate. Primary...

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Gagnadoux, M. F., & Broyer, M. (1995). Oxalosis (Primary Hyperoxaluria). In Inborn Metabolic Diseases (pp. 411–414). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-662-03147-6_40

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