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1. Pierwotna hiperoksaluria typu 1 jako wskazanie do jednoczasowego przeszczepienia wątroby i nerki.

Author

Wicher, Dorota, Jankowska, Irena, Rubik, Jacek, Cielecka-Kuszyk, Joanna, and Pawłowska, Joanna

Subjects
*AUTOSOMAL recessive polycystic kidney, *METABOLIC disorders, *OXALATES, *URINE, *LIVER transplantation, *KIDNEY transplantation
Abstract

The primary hyperoxaluria type 1 (PH1) is an autosomal recessive, inherited disease caused by a defect in glyoxylate metabolism. PH1 is characterized by excessive production and urinary excretion of oxalate that lead to renal and systemic damage through the deposition of oxalate crystals into tissues. Although some patients may benefit from aggressive conservative management the only curative treatment to date is a combined liver-kidney transplantation. [ABSTRACT FROM AUTHOR]

Published
2012

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