Intractable neurological Wilson's disease treated with orthotopic liver transplantation
β Scribed by A. L. Mason; W. Marsh; D. H. Alpers
- Book ID
- 112511152
- Publisher
- Springer US
- Year
- 1993
- Tongue
- English
- Weight
- 677 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0163-2116
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## Abstract We report of a 32βyearβold man who showed dystonic symptoms within few days after liver transplantation (LT). The clinical, biochemical, and, finally, genetic evaluation confirmed Wilson's disease diagnosis in this patient. We suspect that extrapyramidal signs in this case could be a re
A retrospective data analysis on liver transplantation for Wilson's disease (WD) was performed among Italian Liver Transplant Centers. Thirty-seven cases were identified. The main indication for liver transplantation was chronic advanced liver disease in 78% of patients. Mixed hepatic and neuropsych
## Abstract Wilson's disease (WD) is a rare autosomalβrecessive disorder of copper metabolism with predominantly hepatic and extrapyramidal motor symptoms. Copper chelating therapy has proven to be an effective treatment for WD. Yet, if conservative treatment fails, liver transplantation (LT) often