Acute Hepatic Phenotype of Wilson Disease: Clinical Features of Acute Episodes and Chronic Lesions Remaining in Survivors

Background and Aims: Wilson disease (WD) is an inherited disorder of copper metabolism, and an international group for the study of WD (IGSW) has proposed three phenotypes for its initial presentation: acute hepatic, chronic hepatic, and neurologic phenotypes. Characterization of the acute hepatic p...

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Detalles Bibliográficos
Autores principales: Hayashi, Hisao, Tatsumi, Yasuaki, Yahata, Shinsuke, Hayashi, Hiroki, Momose, Kenji, Isaji, Ryohei, Sasaki, Youji, Hayashi, Kazuhiko, Wakusawa, Shinya, Goto, Hidemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Ltd 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721890/
https://www.ncbi.nlm.nih.gov/pubmed/26807378
http://dx.doi.org/10.14218/JCTH.2015.00032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721890/
https://www.ncbi.nlm.nih.gov/pubmed/26807378
http://dx.doi.org/10.14218/JCTH.2015.00032

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