Successful renal transplantation in primary hyperoxaluria.

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Successful renal transplantation in primary hyperoxaluria.

A successful live related renal transplant in a 29-year-old male patient with Type 1 primary hyperoxaluria, who remains well 32 months postoperatively, is described. The plasma oxalate and exchangeable oxalate pool before transplantation were 160 mumol/1 and 4429 mumol respectively. Since the transplant these have been greatly reduced although they remain elevated above the normal by a factor o...

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Primary hyperoxaluria is a rare autosomal recessive disorder, characterised by precipitation of insoluble oxalate crystals in the joints, kidneys, heart, eyes, skin, nerves, and bone marrow. The patients of primary oxaluria usually present with renal stone/nephrocalcinosis, and isolated kidney transplantation should not be done in these patients. We present a case report of 31-year lady with ac...

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Primary hyperoxaluria is a genetic disorder in glyoxylate metabolism that leads to systemic overproduction of oxalate. Functional deficiency of alanine-glyoxylate aminotransferase in this disease leads to recurrent nephrolithiasis, nephrocalcinosis, systemic oxalosis, and kidney failure. We present a young woman with end-stage renal disease who received a kidney allograft and experienced early ...

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Key words: combined liver/kidney transplantation; reference range of 20–40 mmol/l. Prior to analysis, an nephrocalcinosis; primary hyperoxaluria ultrafiltration of plasma to remove proteins and others molecules was performed. Urine ion chromatography was used for measuring urine oxalate concentration with a reference range of

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ژورنال

عنوان ژورنال: Postgraduate Medical Journal

سال: 1980

ISSN: 0032-5473

DOI: 10.1136/pgmj.56.654.288