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The fate of a child with primary hyperoxaluria (oxalosis)
Acta Paediatrica Hungarica
|January 1, 1984
Abstract:
The case of a male child with primary hyperoxaluria type I is reported. In spite of many therapeutic trials, haemodialysis treatment for several years and renal transplantation at the age of 11 years, the patient died after the transplanted kidney had failed.
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