Literature DB >> 29449431

Wilson disease: more than meets the eye.

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


  2 in total

Review 1.  Eye Involvement in Wilson's Disease: A Review of the Literature.

Authors:  Kevin Chevalier; Martine Mauget-Faÿsse; Vivien Vasseur; Georges Azar; Michaël Alexandre Obadia; Aurélia Poujois
Journal:  J Clin Med       Date:  2022-04-30       Impact factor: 4.964

2.  Saccharomyces cerevisiae Concentrates Subtoxic Copper onto Cell Wall from Solid Media Containing Reducing Sugars as Carbon Source.

Authors:  Lavinia L Ruta; Ileana C Farcasanu
Journal:  Bioengineering (Basel)       Date:  2021-03-06
  2 in total

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