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- W2149223852 abstract "Abstract Primary hyperoxaluria is an uncommon, inherited metabolic disorder due to hepatic enzyme deficiencies with consequent hepatic oxalate overproduction and attendant systemic complications. The diagnosis is established on a combination of clinical parameters, elevated urinary excretion of oxalate and glycolate and determination of alanine glyoxylate aminotransferase in the liver tissue. We describe a 45‐year‐old female with end‐stage renal disease secondary to nephrolithiasis, who presented with a fulminating vascular syndrome before confirming the diagnosis of primary hyperoxaluria. This case illustrates that in this infrequent clinical entity, the diagnosis is often delayed with incorrect initial management." @default.
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- W2149223852 date "2009-07-01" @default.
- W2149223852 modified "2023-10-17" @default.
- W2149223852 title "Primary hyperoxaluria causing ESRD and gangrene of extremities leading to amputation" @default.
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- W2149223852 doi "https://doi.org/10.1111/j.1542-4758.2009.00350.x" @default.
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