Hereditary tyrosinemia type 1 in Turkey: Twenty year single-center experience
Date
2015Author
Zeybek, A. Cigdem Aktuglu
Cansever, Serif
Altay, Suheyla
Zubarioglu, Tanyel
Aydin, Ahmet
Erkan, Tulay
Kiykim, Ertugrul
SOYUÇEN, ERDOĞAN
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BackgroundHereditary tyrosinemia type 1(HT1) is a chronic disorder leading to severe hepatic, renal and peripheral nerve damage if left untreated. Despite nitisinone treatment HT1 still carries the risks of hepatocellular carcinoma (HCC) and neuropsychological outcome.
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