A Case Report of a Very Rare Association of Tyrosinemia type I and Pancreatitis Mimicking Neurologic Crisis of Tyrosinemia Type I.

@article{Uar2016ACR,
  title={A Case Report of a Very Rare Association of Tyrosinemia type I and Pancreatitis Mimicking Neurologic Crisis of Tyrosinemia Type I.},
  author={Habibe Koç Uçar and G{\"o}khan T{\"u}mg{\"o}r and Deniz K{\"o}r and Fatih Kardaş and Neslihan {\"O}nenli Mungan},
  journal={Balkan medical journal},
  year={2016},
  volume={33 3},
  pages={370-2}
}
BACKGROUND Tyrosinemia type I is an autosomal recessively inherited metabolic disease of tyrosine metabolism due to the deficiency of fumarylacetoacetate hydrolase. Clinical manifestations include hepatic failure, cirrhosis, hepatocellular carcinoma, renal fanconi syndrome, and neurologic crisis. With the introduction of 2-(2-nitro-4-trifluoro-methylbenzyol… CONTINUE READING