Wilson's disease

音標(biāo)發(fā)音

Wilson's disease is an inherited disorder where there is excessive amounts of copper in the body.
威爾森氏癥是一種遺傳性疾病有過量的銅在體內(nèi)。
Could Edward's changing eye color be a symptom of Wilson's disease, a rare condition that causes the body to retain copper?
（愛德華眼睛變色是否為威爾森氏癥（Wilson’s disease 一種罕見的會導(dǎo)致體內(nèi)銅離子過量的疾?。┑陌Y狀？
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.
結(jié)果：基底節(jié)對稱出現(xiàn)的長T1長T2信號伴腦干病變是本病特征之一，蒼白球T2低信號為本病特征之二；

a genetic disorder in which there is too much copper in the body which damages the liver and nervous system

肝豆?fàn)詈俗冃?p>Methods：128 patients with Wilson's disease from Jan,1983 to Apr,2000 of our hospital were reviewed.
方法：回顧1983-01/2000-04我院128例肝豆?fàn)詈俗冃曰颊叩那闆r，分析比較患者的臨床特點、診斷方法和誤診情況等。
wilson’s病
威爾遜病
威爾遜氏病（遺傳性疾?。?/li>
生物學(xué)
肝豆?fàn)詈俗冃?p>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?fàn)詈俗冃允且环N以銅代謝障礙為特征的常染色體隱性遺傳病，早期干預(yù)有效，因此早期診斷對疾病的預(yù)后有重要意義。
威爾遜氏病
血銅藍(lán)蛋白缺乏病