实用肝脏病杂志 ›› 2015, Vol. 18 ›› Issue (1): 89-91.doi: 10.3969/j.issn.1672-5069.2015.01.026

• 综述 • 上一篇    下一篇

特殊人群肝豆状核变性诊治进展*

曹海霞 综述, 范建高 审校   

  1. 200092 上海市 上海交通大学医学院附属新华医院消化内科
  • 收稿日期:2014-05-07 出版日期:2015-12-17 发布日期:2015-12-17
  • 通讯作者: 范建高,E-mail:fanjiangao@gmail.com E-mail:caohaixia204106@126.com
  • 作者简介:曹海霞,女,32岁,博士研究生,主治医师。主要从事慢性肝病的防治研究。E-mail:caohaixia204106@126.com
  • 基金资助:
    上海交通大学医学院基金(编号:13XJ10021); 中国肝炎防治基金会资助项目(编号:cfhpc20132061)

What is special in patients with Wilson's disease in children and pregnant women

Cao Haixia, Fan Jiangao   

  1. Department of Gastroenterology,Xinhua Hospital,Shanghai Jiaotong University School of Medicine,Shanghai 200092,China
  • Received:2014-05-07 Online:2015-12-17 Published:2015-12-17

摘要: 肝豆状核变性的临床表现具有异质性,早期诊断较难,容易漏诊。尽管肝豆状核变性是一种遗传代谢性疾病,但若能早期诊断,根据患者的临床特点制定治疗方案,治疗效果较佳,长期预后较好。妊娠、儿童、急性肝衰竭等特殊人群的治疗仍是临床医生关注的热点问题。

关键词: 肝豆状核变性, 诊断, 治疗, 急性肝衰竭

Abstract: The clinical manifestations of Wilson's disease appear to be variable and it is sometimes difficult to diagnose at early stage. Although it is a genetic disorder of copper metabolism, if discovered early,effective treatments are available and the prognosis is good. The management of this disease in pregnant women, children and patient with acute liver failure,is highly concerned in clinical practice.

Key words: Wilson's disease, Diagnosis, Treatment, Acute liver failure