Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases

doi:10.4254/wjh.v5.i3.156

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Mar 27, 2013 (publication date) through Aug 31, 2024

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World Journal of Hepatology

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1948-5182

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Hepatol. Mar 27, 2013; 5(3): 156-159
Published online Mar 27, 2013. doi: 10.4254/wjh.v5.i3.156

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Figure 1 Histological findings. Biopsy specimen showing mild lobular activity, mild portoperiportal activity and periportal fibrosis with frequent portal to portal bridging fibrosis. A: Masson’s Trichrome stain, 40×; B: Masson’s Trichrome stain, 400×.

Citation: Kim JW, Kim JH, Seo JK, Ko JS, Chang JY, Yang HR, Kang KH. Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases. World J Hepatol 2013; 5(3): 156-159
URL: https://www.wjgnet.com/1948-5182/full/v5/i3/156.htm
DOI: https://dx.doi.org/10.4254/wjh.v5.i3.156