戈谢病

而过量表达cathepsinK会引起戈谢病（Gaucher病）。

Overexpression of cathepsin K can cause Gaucher disease .

酶替代疗法治疗Norrbottnian（3型）戈谢病的10年随访研究

Ten years'experience of enzyme infusion therapy of Norrbottnian ( type 3 ) Gaucher disease

酶替代治疗戈谢病72例

A retrospective study on enzyme replacement therapy in patients with Gaucher disease

以不自主运动为表现的戈谢病报告并文献复习

Gaucher Disease with Involuntary Movement : A Case Report and Review of Literature

根据国际戈谢病组织统计，2500美国人患有戈谢病。

According to the national Gaucher foundation , 2500 Americans suffer from Gaucher disease .

戈谢病是一种遗传性疾病，是由缺乏一种名为葡萄糖脑苷脂酶的酶引起的。

Gaucher disease is an inherited disorder that is caused by a deficiency in an enzyme called glucocerebrosidase .

戈谢病会导致疼痛、疲劳、黄疸、骨髓的破坏、贫血甚至死亡。

Gaucher disease can result in pain , fatigue , jaundice , bone damage , anemia , and even death .

键赞公司建立这个网站是为了与戈谢病患者共同生活者或者照料者，包括专业护理员。

Genzyme has created this website for people living with or caring for someone with Gaucher disease , including health care professionals .

在德系犹太人中，戈谢病是最普遍的基因突变疾病，大约为1/450。

Among the Ashkenazi Jewish population , Gaucher disease is the most common genetic disorder , with an incidence of approximately 1 in 450 persons .

戈谢病是一种由基因突变引起的疾病。这种冲突变成了思想交流而不是争吵。

Gaucher ( pronounced " go-SHAY ") disease is an inherited illness caused by a gene mutation . This type of conflict becomes an exchange of ideas instead of a quarrel .