Tyrosinemia Type I and Reversible Neurogenic Crisis After a One-Month Interruption of Nitisinone

Hereditary tyrosinemia Type I (HTI) is an autosomal recessive disorder due to a deficiency of the enzyme fumarylacetoacetate hydrolase. The liver is the primary organ that is affected and comorbidities with renal and neurologic systems and hepatocellular carcinoma can be seen as a long-term complica...

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Bibliographic Details
Main Authors: Havva Yazıcı, Ebru Canda, Esra Er, Mehmet Arda Kılınç, Sema Kalkan Uçar, Bülent Karapınar, Mahmut Çoker
Format: Article
Language:English
Published: Galenos Yayinevi 2018-03-01
Series:Journal of Pediatric Research
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Online Access: http://jpedres.org/archives/archive-detail/article-preview/tyrosinemia-type--and-reversible-neurogenic-crisis/18786

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