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Rapid Diagnosis of Wilson Disease in Acute Liver Failure: No More Waiting for the Ceruloplasmin Level?

机译:急性肝衰竭中威尔逊病的快速诊断:不再需要血浆铜蓝蛋白水平了吗?

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摘要

The findings in this issue of HEPATOLOGY from Kor-man et al. (from the Pediatric and Adult Acute Liver Failure Study Groups, National Institutes of Health) are therefore of considerable interest because they demonstrate that there is no actual need to wait for specific biochemical tests of deranged copper metabolism, such as ceruloplasmin or copper, that are not often rapidly available. Previous studies that have attempted to define simple biochemical testing for the diagnosis of fulminant WD have been hampered by their small patient numbers due the rarity of this condition (overall prevalence 1:30,000).
机译:Kor-man等人在本期肝病学中的发现。 (来自美国国立卫生研究院儿科和成人急性肝衰竭研究小组)因此引起了极大的兴趣,因为它们表明实际上并不需要等待对铜代谢异常的特定生化测试,例如铜蓝蛋白或铜。往往无法迅速获得。以前的研究试图定义简单的生化测试以诊断暴发性WD,但由于这种病的罕见性,其患者人数很少(总患病率为1:30,000)。

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