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- W2043955108 abstract "Primary hyperoxaluria is a rare, inherited metabolic disease caused by enzymatic defect of glyoxilate carboligase or D-glyceric dehydrogenase. The disease leads to overproduction of oxalic acid and deposition of calcium oxalate crystals in organs and tissues (oxalosis). In this report, we describe a case of primary hyperoxaluria in a 26-year-old female. We wish to report the main features of the disorder and to underline the severe bony lesions." @default.
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- W2043955108 date "1990-05-01" @default.
- W2043955108 modified "2023-09-23" @default.
- W2043955108 title "Primary hyperoxaluria: a report of a case" @default.
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- W2043955108 doi "https://doi.org/10.1016/0720-048x(90)90140-7" @default.
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