Authors
Huy P Pham, Joseph Schwartz, Laura Cooling, Jan C Hofmann, Haewon C Kim, Shanna Morgan, Monica B Pagano, Jennifer Schneiderman, Jeffrey L Winters, Chisa Yamada, Edward CC Wong, Yanyun Wu
Publication date
2016/2
Journal
Journal of clinical apheresis
Volume
31
Issue
1
Pages
11-15
Description
Purpose
Wilson's disease is a rare autosomal recessive genetic disorder that results in accumulation of copper in the liver, brain, cornea and kidney. Therapeutic plasma exchange (TPE) has been used to remove copper and provide a bridge to liver transplantation. We report here the collective experiences through the ASFA apheresis registry on Wilson's disease.
Methods
The ASFA apheresis registry is a multi‐center registry study. Both prospective and retrospective data, with the latter involving data collection back to January 2000 are entered in the registry. The registry includes patient demographics, apheresis procedural information, treatment schedules, and treatment outcomes and complications.
Results
A total of 10 patients (3 males and 7 females) with Wilson's disease treated between 2005 and 2013 were included. Median age of first diagnosis and first TPE were 16 and 17 years, respectively. Via …
Total citations
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Scholar articles
HP Pham, J Schwartz, L Cooling, JC Hofmann, HC Kim… - Journal of clinical apheresis, 2016