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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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Bibliografski detalji
Glavni autori:	Umapati Hegde (Autor), Rajapurkar Mohan (Autor), Gang Sishir (Autor), Amit Jojera (Autor), Shailesh Soni (Autor)
Format:	Knjiga
Izdano:	Archives of Clinical Nephrology - Peertechz Publications, 2021-01-18.
Teme:	Case Report
Online pristup:	Connect to this object online.
Oznake:	Dodaj oznaku Bez oznaka, Budi prvi tko označuje ovaj zapis!

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