Crystalline nephropathy due to adenine phosphoribosyl transferase deficiency as a cause of renal allograft dysfunction
<p>APRT deficiency is a rare but under recognized genetic disease. </p><p>Recurrent urolithiasis and DHA nephropathy are the two clinical manifestations of APRT deficiency and diagnosis can be made at any age and recurs after renal transplant. Allopurinol is the cornerstone in prev...
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| Main Authors: | , , , , |
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| Format: | Book |
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Archives of Clinical Nephrology - Peertechz Publications,
2021-01-18.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |