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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
Published online Mar 27, 2013. doi: 10.4254/wjh.v5.i3.156
Table 1 Clinical and biochemical features of the patient
| Age (mo) | 9 | 22 | 23 | 24 | 26 | 27 | 30 |
| AST/ALT (IU/L) | 102/122 | 113/144 | 90/105 | 171/194 | 185/285 | 262/401 | 111/162 |
| Cu in urine (μg/24 h) | 14.9 | 15.2 | 62.2 | 421.4 | |||
| Ceruloplasmin (mg/dL) | < 9 | < 9 | < 8 | < 8 | |||
| Mutation | p.G1186S/c.4006delA | ||||||
| K-F ring | No | ||||||
| Cu in the liver (μg/g dry weight) | 748 | ||||||
- 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