• For example, the hereditary hemochromatosis mutation protects carriers from iron-deficiency because the mutated gene allows increased efficiency of iron absorption.

    例如因为突变基因可以提高吸收效率所以遗传性血色素沉着病突变可以保护带菌者不缺铁。

    youdao

  • The term "hemochromatosis" is used when organ dysfunction occurs.

    发生器官功能障碍时,则血色素沉着症”表示。

    youdao

  • Bronze hyperpigmentation is seen in hemochromatosis and arsenic intoxication.

    青铜色的色素沉着见于血色素沉着症中毒。

    youdao

  • Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.

    结节肝硬化可见Wilson原发性胆汁硬化血色素沉着症

    youdao

  • HHC results from a mutation involving the hemochromatosis gene (HFE) that leads to increased iron absorption from the gut.

    该病是由于血色素沉着基因(HFE)突变使得肠吸收增加所致。

    youdao

  • Hemochromatosis, with excessive iron deposition, can occur in the heart as shown here microscopically with Prussian blue iron stain.

    血色素沉着症是由于过度沉积而引起的。如图所示,经过普鲁士蓝铁染色后可见该病显微镜下的表现。

    youdao

  • Hemochromatosis gene, associated with a disease that leads to excessive iron accumulation, may also influence the absorption of lead.

    血色基因引起过量蓄积而致病影响吸收

    youdao

  • One dolphin that had especially high insulin levels compared to others, also had a 10-year history of iron overload, or hemochromatosis.

    其中一只的胰岛素水平明显高于其他五只。这一只海豚患有负荷血色沉着病。

    youdao

  • The Prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis (HH).

    普鲁士染色显示遗传性血色素沉着症(HH)患者镜下可见广泛肝脏铁血黄素沉着。

    youdao

  • Objective to observe the ultrastructural changes of skin and compositions of fine structures in the cytoplasm in the patients with secondary hemochromatosis.

    目的观察继发性血色病患者皮肤超微变化微细构造元素组成

    youdao

  • The excessive deposition of iron leads to heart enlargement and failure similar to a cardiomyopathy, making hemochromatosis a form of "restrictive" cardiomyopathy.

    过度沉淀导致心脏增大以及类似心肌病心力衰竭,这使得血色素沉着症成为限制性心肌病一种形式

    youdao

  • Objective to investigate the prevalence of the C282Y mutation in the HFE gene associated with hereditary hemochromatosis (HH) in the Henan Han population in China.

    目的调查中国河南汉族人遗传性血色素沉着症hfe C282Y基因突变情况。

    youdao

  • HEMOCHROMATOSIS - a genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure.

    血色沉着病——一种遗传性病症引起胃肠道吸收增多沉积肝脏导致最终肝硬化衰竭

    youdao

  • HEMOCHROMATOSIS - a genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure.

    血色沉着病——一种遗传性病症引起胃肠道吸收增多沉积肝脏导致最终肝硬化衰竭

    youdao

$firstVoiceSent
- 来自原声例句
小调查
请问您想要如何调整此模块?

感谢您的反馈,我们会尽快进行适当修改!
进来说说原因吧 确定
小调查
请问您想要如何调整此模块?

感谢您的反馈,我们会尽快进行适当修改!
进来说说原因吧 确定