Recurrent Hemolytic Anemia as an Inaugural Manifestation of Wilson Disease in Children: A Case Report

O. Louachama, A. Bourrahouat, Ibtissam Khattou, I. A. Sab, M. Sbihi
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Abstract

Wilson disease (WD) is a disorder of copper metabolism. Liver and brain disorders are the main presentations, hemolytic anemia in WD is a rare inaugural symptom. We report a case of a child who developed recurrent hemolytic anemia associated with liver failure in the second hemolysis episode as the first manifestation of WD. Wilson's disease is not exceptional in children with hemolytic anemia, but another differential diagnosis must be excluded.
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复发性溶血性贫血是儿童肝豆状核病的首要表现:1例报告
威尔逊病(WD)是一种铜代谢障碍。肝脑功能障碍是主要的表现,溶血性贫血是一个罕见的首发症状。我们报告一个病例的儿童谁发展复发性溶血性贫血与肝功能衰竭在第二次溶血发作作为WD的第一表现。威尔逊氏病在儿童溶血性贫血中并不少见,但必须排除其他鉴别诊断。
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