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躰內(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爲(wèi)威爾森氏癥（Wilson’s disease 一種罕見的會(huì)導(dǎo)致躰內(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(duì)稱出現(xiàn)的長(zhǎng)T1長(zhǎng)T2信號(hào)伴腦乾病變是本病特征之一，蒼白球T2低信號(hào)爲(wèi)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：廻顧1983-01/2000-04我院128例肝豆?fàn)詈俗冃曰颊叩那闆r，分析比較患者的臨牀特點(diǎn)、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以銅代謝障礙爲(wèi)特征的常染色躰隱性遺傳病，早期乾預(yù)有傚，因此早期診斷對(duì)疾病的預(yù)後有重要意義。
威爾遜氏病
血銅藍(lán)蛋白缺乏病