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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Detalles Bibliográficos
Autores principales: Dehghani, Seyed Mohsen, Haghighat, Mahmood, Imanieh, Mohammad Hadi, Karamnejad, Hossein, Malekpour, Abdorrasoul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898443/
https://www.ncbi.nlm.nih.gov/pubmed/24498493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898443/
https://www.ncbi.nlm.nih.gov/pubmed/24498493

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