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Tyrosinemia and Liver Transplantation: Experience at CHU Sainte-Justine
Fernando Alvarez1, Grant A Mitchell2
1Service de gastroentérologie, hépatologie et nutrition, CHU Sainte-Justine, Université de Montréal, 3175 chemin Côte-Sainte-Catherine, Montréal, Québec, H3T 1C5, Canada. fernando.alvarez@umontreal.ca.
Abstract:
Tyrosinemia is a disease of the tyrosine metabolism, affecting mainly liver, kidney and peripheral nerves. Two forms of liver disease caused by a deficiency of FAH are recognised: (1) acute liver failure; (2) chronic liver disease. Since the introduction of NTBC [2-(2-nitro-4-trifluoromethyl benzoyl)-1-3-cyclohexanedione] (nitisinoneR) in the treatment of tyrosinemia, no liver disease has been observed when started in the first weeks of life. Liver transplantation is a good option for the treatment of tyrosinemic patients developing liver nodules, with high suspicion of hepatocarcinoma. In the long-term outcome of the liver transplant, survival was of 90% in tyrosinemic patients.
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