变性(医学)
怀孕
病态的
威尔逊病
疾病
医学
排泄
内科学
病理
生理学
生物
遗传学
作者
Jie Bai,Sujun Zheng,Z P Duan
出处
期刊:PubMed
[National Institutes of Health]
日期:2022-01-20
卷期号:30 (1): 107-109
被引量:1
标识
DOI:10.3760/cma.j.cn501113-20200807-00441
摘要
Hepatolenticular degeneration (Wilson's disease, WD) is a kind of autosomal recessive genetic disease characterized by disorders of copper metabolism. It is caused by mutations in the ATP7B gene, resulting in impaired excretion of copper into the bile, and then pathological deposition in the liver, brain, and other organs. Early diagnosis and treatment can significantly improve the prognosis of patients with WD. However, there is still no clear consensus on the treatment and management of WD during pregnancy. Herein, the clinical management of WD during pregnancy is summarized for clinicians' reference.
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