| Literature DB >> 29449431 |
Claire Kelly1,2, Marinos Pericleous1,2.
Abstract
Wilson disease is a rare but important disorder of copper metabolism, with a failure to excrete copper appropriately into bile. It is a multisystem condition with presentations across all branches of medicine. Diagnosis can be difficult and requires a high index of suspicion. It should be considered in unexplained liver disease particularly where neuropsychiatric features are also present. Treatments are available for all stages of disease. A particularly important presentation not to overlook is acute liver failure which carries a high mortality risk and may require urgent liver transplantation. Here, we provide an overview of this complex condition. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: copper metabolism; hepatology; movement disorder
Mesh:
Year: 2018 PMID: 29449431 DOI: 10.1136/postgradmedj-2017-135381
Source DB: PubMed Journal: Postgrad Med J ISSN: 0032-5473 Impact factor: 2.401