Wilson's disease
音标发音
- 英式音标 [ˈwɪl.sənz dɪˌziːz]
- 美式音标 [ˈwɪl.sənz dɪˌziːz]
- 英式发音
- 美式发音
基本解释
- [医] 威尔逊氏病（遗传性疾病）
英汉例句
- Wilson's disease is an inherited disorder where there is excessive amounts of copper in the body.
威尔森氏症是一种遗传性疾病有过量的铜在体内。 - Could Edward's changing eye color be a symptom of Wilson's disease, a rare condition that causes the body to retain copper?
（爱德华眼睛变色是否为威尔森氏症（Wilson’s disease 一种罕见的会导致体内铜离子过量的疾病）的症状？ - Results: MRI showed long T1, long T2 in bilateral basal ganglia and brain stem was one of the feature of Wilson's disease, another was low signals on T2WI.
结果：基底节对称出现的长T1长T2信号伴脑干病变是本病特征之一，苍白球T2低信号为本病特征之二；
双语例句
词组短语
- Wilson 's disease 肝豆状核变性;威尔森氏症;流式细胞仪;威尔森氏病
- wilson ' s disease gene 病基因
- Kinnier -Wilson's disease 金
短语
英英字典
- a genetic disorder in which there is too much copper in the body which damages the liver and nervous system
剑桥英英字典
专业释义
- 肝豆状核变性
Methods：128 patients with Wilson's disease from Jan,1983 to Apr,2000 of our hospital were reviewed.
方法：回顾1983-01/2000-04我院128例肝豆状核变性患者的情况，分析比较患者的临床特点、诊断方法和误诊情况等。 - wilson’s病
- 威尔逊病
- 威尔逊氏病（遗传性疾病）
- 肝豆状核变性
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism. Early diagnosis is important since it can be effectively treated if diagnosis can be made in early life.
肝豆状核变性是一种以铜代谢障碍为特征的常染色体隐性遗传病，早期干预有效，因此早期诊断对疾病的预后有重要意义。 - 威尔逊氏病
- 血铜蓝蛋白缺乏病