Combined liver and kidney transplantation in primary hyperoxaluria: A report of three cases and review of the literature

Combined liver and kidney transplantation in primary hyperoxaluria: A report of three cases and review of the literature

Primary hyperoxaluria type-1 (PH-1) is a rare autosomal recessive metabolic disorder leading to excessive oxalate production, deposition of calcium oxalate crystals in the kidney, nephrocalcinosis, progressive renal failure and systemic deposition of oxalate (oxalosis). Combined liver and kidney tra...

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Bibliographic Details
Main Authors: Prasad Nair, Torki Al-Otaibi, Narayanan Nampoory, Wafa′a Al-Qabandi, Tarek Said, Medhat Abdul Halim, Osama Gheith
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Saudi Journal of Kidney Diseases and Transplantation
Online Access:http://www.sjkdt.org/article.asp?issn=1319-2442;year=2013;volume=24;issue=5;spage=969;epage=975;aulast=Nair

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http://www.sjkdt.org/article.asp?issn=1319-2442;year=2013;volume=24;issue=5;spage=969;epage=975;aulast=Nair

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