Case of hepatocellular carcinoma in a patient with hereditary tyrosinemia in the post-newborn screening era

Hereditary tyrosinemia type 1 (HT-1) is a metabolic disorder caused by a defect in tyrosine degradation. Without treatment, symptoms of hepatomegaly, renal tubular dysfunction, growth failure, neurologic crises resembling porphyrias, rickets and possible hepatocellular carcinoma can develop. The use...

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Detalles Bibliográficos
Autores principales: Imseis, Essam M, Bynon, John S, Thornhill, Chad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368626/
https://www.ncbi.nlm.nih.gov/pubmed/28396719
http://dx.doi.org/10.4254/wjh.v9.i9.487

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368626/
https://www.ncbi.nlm.nih.gov/pubmed/28396719
http://dx.doi.org/10.4254/wjh.v9.i9.487

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