Therapeutic plasmapheresis as a bridge to liver transplantation in fulminant Wilson disease
Wilson disease is an autosomal recessive disorder of copper metabolism that leads to the accumulation of copper mainly in the liver, cornea, brain, and kidney. Rarely, Wilson disease can present as fulminant hepatic failure with direct antiglobulin test–negative hemolytic anemia and renal failure. I...
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Published in | Journal of clinical apheresis Vol. 22; no. 1; pp. 10 - 14 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.02.2007
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Subjects | |
Online Access | Get full text |
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