例如,因为突变的基因可以提高铁的吸收效率,所以遗传性血色素沉着病突变可以保护带菌者不缺铁。
For example, the hereditary hemochromatosis mutation protects carriers from iron-deficiency because the mutated gene allows increased efficiency of iron absorption.
青铜色的色素沉着见于血色素沉着症和砷中毒。
Bronze hyperpigmentation is seen in hemochromatosis and arsenic intoxication.
当发生器官功能障碍时,则用“血色素沉着症”表示。
The term "hemochromatosis" is used when organ dysfunction occurs.
该病是由于血色素沉着症基因(HFE)突变使得肠吸收铁增加所致。
HHC results from a mutation involving the hemochromatosis gene (HFE) that leads to increased iron absorption from the gut.
小结节型肝硬化也可见于Wilson病、原发性胆汁硬化和血色素沉着症。
Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.
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。
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.
普鲁士蓝铁染色显示,遗传性血色素沉着症(HH)患者在镜下可见广泛的肝脏含铁血黄素沉着。
The Prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis (HH).
血色素沉着症是由于铁过度的沉积而引起的。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。
Hemochromatosis, with excessive iron deposition, can occur in the heart as shown here microscopically with Prussian blue iron stain.
铁的过度沉淀可导致心脏增大以及类似心肌病的心力衰竭,这使得血色素沉着症成为限制性心肌病的一种形式。
The excessive deposition of iron leads to heart enlargement and failure similar to a cardiomyopathy, making hemochromatosis a form of "restrictive" cardiomyopathy.
铁的过度沉淀可导致心脏增大以及类似心肌病的心力衰竭,这使得血色素沉着症成为限制性心肌病的一种形式。
The excessive deposition of iron leads to heart enlargement and failure similar to a cardiomyopathy, making hemochromatosis a form of "restrictive" cardiomyopathy.
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