scholarly journals Liver Failure with Coagulopathy, Hyperammonemia and Cyclic Vomiting in a Toddler Revealed to Have Combined Heterozygosity for Genes Involved with Ornithine Transcarbamylase Deficiency and Wilson Disease

Author(s):  
Valerie Mira ◽  
Richard G. Boles
2017 ◽  
pp. 17-22 ◽  
Author(s):  
Farrah Rajabi ◽  
Lance H. Rodan ◽  
Maureen M. Jonas ◽  
Janet S. Soul ◽  
Nicole J. Ullrich ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (4) ◽  
pp. e0153358 ◽  
Author(s):  
Alexander Laemmle ◽  
Renata C. Gallagher ◽  
Adrian Keogh ◽  
Tamar Stricker ◽  
Matthias Gautschi ◽  
...  

2021 ◽  
Vol 11 (01) ◽  
pp. e145-e147
Author(s):  
Nida Mirza ◽  
Ravi Bharadwaj ◽  
Smita Malhotra ◽  
Anupam Sibal

AbstractWilson disease (WD) is a disorder of copper metabolism resulting in accumulation of copper in vital organs of the human body, predominantly in the liver and the brain. Acute liver failure in WD has a bad prognosis, especially with a score ≥11 in the revised WD prognostic index; emergency liver transplantation is considered the only life-saving option in this scenario. Here, we reported a girl patient with WD-induced liver failure and poor prognostic score who was rescued by plasmapheresis. She also manifested severe Coombs negative hemolytic anemia and acute kidney injury. This case report highlights the utility of an adjunctive modality besides liver transplantation for the management of fulminant liver failure caused by WD.


2009 ◽  
Vol 53 (1) ◽  
pp. 100-102 ◽  
Author(s):  
Lakshmi Venkateswaran ◽  
Fernando Scaglia ◽  
Valerie McLin ◽  
Paula Hertel ◽  
Oleg A. Shchelochkov ◽  
...  

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