Late-onset Wilson Disease in a Patient Followed-up for Nonalcoholic Fatty Liver Disease
Author:
Affiliation:
1. Department of Gastroenterology, Saitama Medical Center, Jichi Medical University, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/63/1/63_1789-23/_pdf
Reference21 articles.
1. 1. Sandahl TD, Laursen TL, Munk DE, Vilstrup H, Weiss KH, Ott P. The prevalence of Wilson's disease: an update. Hepatology 71: 722-732, 2020.
2. 2. Wallace DF, Dooley JS. ATP7B variant penetrance explains differences between genetic and clinical prevalence estimates for Wilson disease. Hum Genet 139: 1065-1075, 2020.
3. 3. Yamaguchi H, Nagase H, Tokumoto S, et al. Prevalence of Wilson disease based on genome databases in Japan. Pediatr Int 63: 918-922, 2021.
4. 4. Shimizu N, Suzuki M, Yamaguchi Y, Aoki T, Matsuda I, Arima M. [A nation-wide survey for neurologic and hepato-neurologic type of Wilson disease: clinical features and hepatic copper content]. No To Hattatsu 28: 391-397, 1996 (in Japanese, Abstract in English).
5. 5. Ferenci P, Czlonkowska A, Merle U, et al. Late-onset Wilson's disease. Gastroenterology 132: 1294-1298, 2007.
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1. A Case of Wilson's Disease Suspected to Involve a Novel Genetic Mutation of ATP7B Gene, Requiring a Differential Diagnosis with Non-alcoholic Steatohepatitis;Internal Medicine;2024
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