Clinical and para clinical findings in the children with tyrosinemia referring for liver transplantation

Clinical and para clinical findings in the children with tyrosinemia referring for liver transplantation

Background: Hereditary tyrosinemia type 1 (HT1) is a rare autosomal recessive inborn error of metabolism caused by deficiency of fumarylacetoacetate hydrolase enzyme. This disease manifests with severe liver and kidney impairment and is associated with an increased risk of liver cancer. The aim of t...

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Bibliographic Details
Main Authors: Seyed Mohsen Dehghani, Mahmood Haghighat, Mohammad Hadi Imanieh, Hossein Karamnejad, Abdorrasoul Malekpour
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:International Journal of Preventive Medicine
Subjects:
Liver transplantation
newborn screening
succinylacetone
tyrosinemia
Online Access:http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2013;volume=4;issue=12;spage=1380;epage=1385;aulast=Dehghani

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http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2013;volume=4;issue=12;spage=1380;epage=1385;aulast=Dehghani

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