Wilson's Disease: A Rare and Enigmatic Disease

被引：0
|
作者：
Xu, Guang [1 ]
Geiger, Joseph L. [1 ]
Pfaff, Sean J. [2 ]
机构：
[1] Marian Univ, Wood Coll Osteopath Med, Indianapolis, IN 46222 USA
[2] Indiana Univ, Sch Med, Dept Radiol & Imaging Sci, Indianapolis, IN USA
来源：
CLINICAL & TRANSLATIONAL METABOLISM | 2024年 / 22卷 / 01期
关键词：
D O I：
10.1007/s12018-024-09301-7
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The comprehensive review by Lafhal and Fdil provides overview of the pathophysiology, clinical features, and different diagnostic strategies for Wilson's disease (WD), a rare and serious hereditary disorder of copper metabolism. The variable clinical manifestations of WD and the lack of a single definitive test presents significant diagnostic challenges.
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页数：2
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