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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Bibliografiske detaljer
Main Authors: Dehghani, Seyed Mohsen, Haghighat, Mahmood, Imanieh, Mohammad Hadi, Karamnejad, Hossein, Malekpour, Abdorrasoul
Format: Artigo
Sprog:Inglês
Udgivet: Medknow Publications & Media Pvt Ltd 2013
Fag:
Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3898443/
https://ncbi.nlm.nih.gov/pubmed/24498493
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