hemochromatosis
n.
血色沉着病；
英英释义
hemochromatosis[ 'hi:mə,krəumə'təusis, 'he- ]
n.pathology in which iron accumulates in the tissues; characterized by bronzed skin and enlarged liver and diabetes mellitus and abnormalities of the pancreas and the joints
同义词：iron-storage diseaseiron overloadbronzed diabetes
权威例句
Hereditary hemochromatosis--a new look at an old diseaseHemochromatosis and iron-overload screening in a racially diverse population.
Long-term survival in patients with hereditary hemochromatosis.
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
A Population-Based Study of the Clinical Expression of the Hemochromatosis Gene
Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor.
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
Mutations in HFE2 cause iron overload in chromosome 1q|[ndash]|linked juvenile hemochromatosis
Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis
Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis.
1. 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。
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2. The term "hemochromatosis" is used when organ dysfunction occurs.
当发生器官功能障碍时，则用“血色素沉着症”表示。
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3. 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和砷中毒。
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4. Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.
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。
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5. 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症基因(HFE)突变使得肠吸收铁增加所致。
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6. 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。
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7. Hemochromatosis gene, associated with a disease that leads to excessive iron accumulation, may also influence the absorption of lead.
血色病基因可引起铁的过量蓄积而致病，也会影响到铅的吸收。
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8. One dolphin that had especially high insulin levels compared to others, also had a 10-year history of iron overload, or hemochromatosis.
其中有一只的胰岛素水平明显高于其他五只。这一只海豚还患有铁负荷、血色沉着病。
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9. The Prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis (HH).
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。
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10. 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和微细构造的元素组成。
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11. 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。
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12. 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。
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13. 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铁增多，沉积在肝脏，导致最终肝硬化或肝衰竭。
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14. 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铁增多，沉积在肝脏，导致最终肝硬化或肝衰竭。
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hemochromatosis
