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

• Auteurs principaux: Havva Yazıcı (Auteur), Ebru Canda (Auteur), Esra Er (Auteur), Mehmet Arda Kılınç (Auteur), Sema Kalkan Uçar (Auteur), Bülent Karapınar (Auteur), Mahmut Çoker (Auteur)
• Format: Livre
• Publié: Galenos Yayinevi, 2018-03-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

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...