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Late diagnosed Wilson disease with hepatic and neurological manifestations

✍ Scribed by Yuichi Honma; Masaru Harada; Miyuki Sato; Yuka Katsuki; Masaaki Hiura; Michihiko Shibata; Ryoichi Narita; Riko Harada; Shintaro Abe; Akinari Tabaru; Nobuyoshi Tajiri; Shohei Shimajiri

Book ID: 118088367
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 997 KB
Volume: 41
Category: Article
ISSN: 1386-6346
DOI: 10.1111/j.1872-034x.2010.00754.x

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## Abstract Wilson's disease (WD) is a rare autosomal‐recessive 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