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

1 Jan 2013

Abstract excerpt

Wilson disease (WD) is an autosomal recessive disorder of copper transport caused by alteration of the adenosine triphosphatase 7B gene. It is rare to diagnose WD below the age of three years. Molecular genetic testing is one of the most important diagnostic methods and may confirm the diagnosis in equivocal cases. We report a case of a 9-mo old boy with WD who presented as chronic hepatitis. Genetic analysis...

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PMID: 23556051
DOI: 10.4254/wjh.v5.i3.156

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