hemochromatosis

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.

Materials and methods: Hepatic CT scaning was performed in 4 patients with hemochromatosis.

材料与方法：4例血色病患者行肝脏CT平扫。

Hemochromatosis, the common autosomal recessive disease of iron overload, affects at least 1 in 300 Caucasians.

遗传性血色素沉着症是一种常染色体隐性遗传性铁异常沉积性疾病，高加索群体中发病率高，平均不到300人就有一个是该病患者。

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.

The results of genetic analysis in this disease group suggest that hemochromatosis is an autosomal dominant inheritance but not autosomal recessive inheritance disease.

本组病例遗传方式分析结果，不支持常染色体隐性遗传，确定为常染色体显性遗传。

Relationship between HFE gene and hereditary hemochromatosis

HFE基因与遗传性血色素沉着症

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。

HFE gene is a major histocompatibility complex class ⅰ-like gene, which was identified as a candidate gene for hemochromatosis in 1996. The proposed role for HFE is its part in the regulation of the interaction of the transferrin receptor with transferrin.

HFE基因发现于1996年，属于HLA类样基因，是遗传性血色素沉着症候选基因。HFE分子的功能可能是参与调节转铁蛋白与转铁蛋白受体间的相互作用。

we suggest that hemochromatosis should be considered in the differential diagnosis of hydrops fetalis.

我们建议，血色病中应考虑的鉴别诊断胎儿水肿。

Genetic epidemiology and HLA survey of primary hemochromatosis among Chinese Miao ethnic

中国苗族人群原发性血色病的遗传流行病学调查及HLA研究

Hemochromatosis is a disorder of iron metabolism of the body of a genetic disease.

血色病是因组织中铁的沉积过多而发生的全身性疾病。

Application of Electron Microscopic X-ray Microanalysis in Secondary Hemochromatosis

电镜X射线显微分析法在继发性血色病研究中的运用

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。

These genes are δ aminolevulinic acid dehydratase ( ALAD) gene, vitamin D receptor ( VDR) and hemochromatosis gene. Their relation to susceptibility to lead poisoning in humans was reviewed in this paper.

δ氨基γ酮戊酸脱水酶基因、维生素D受体基因及血色素沉着病基因等遗传多态性可能造成儿童对铅毒性作用有不同的易感性，本文就此进行综述。

FERRITIN-Iron-containing serum protein measured by laboratory to help establish a diagnosis of hemochromatosis.

铁蛋白 —— 含铁的血清蛋白,由实验室血液检测帮助诊断血色沉着病.

Metabolic diseases such as Wilson's disease, hemochromatosis, and alpha 1-antitrypsin deficiency can lead to liver damage.

代谢性疾病,如威尔逊氏病, 血色沉着, α -1 型胰岛素缺乏症均可导致肝损伤.

It has a higher incidence in postnecrotic cirrhosis and hemochromatosis than in Laennec's cirrhosis.

坏死后肝硬变及血色素沉着症引起的肝癌比门脉性肝硬变所引起者为多.

Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes

青少年血红蛋白沉积症伴随成人血红蛋白沉积症基因的病理性突变

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。

Iron deficiency can cause iron deficiency anemia ( IDA) and neurological diseases of children, whereas iron overload can cause hemochromatosis.

铁缺乏可以引起缺铁性贫血和儿童神经系统的疾病，铁过载可以引起血色病。

Ultrastructural study of iron deposition in liver of hemochromatosis patient

血色病病人肝内铁沉积点的超微结构研究

"For example, hemochromatosis is a deadly disease that can cause liver failure or liver cancer. When the disease is found early, it can be cured."

例如，血色素沉着症是一种能引起肝衰竭或者肝癌的致命疾

He could have had hemochromatosis.

他应该得了血色沉着病。

One Case: Primary Idiopathic Hemochromatosis

肝原发性特发性血色素沉着症1例报告

Hepatic iron overload in hemochromatosis: a case report

血色病肝脏铁过度沉着症1例

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。

Survival after liver transplantation in patients with hepatic iron overload: The National Hemochromatosis Transplant Registry

肝脏铁超载患者肝移植后的生存率：国家血红蛋白沉积症肝移植注册

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。

Hemochromatosis with secondary diabetes mellitus: one case report

原发性血色病继发性糖尿病一例报告

Objective To study the clinical characteristics of hereditary hemochromatosis ( HHC) and to evaluate the effect of clinical examination in HHC early diagnosis.

目的探讨遗传性血色病的临床特点，评价铁生化指标、MRI、肝穿病理学检查在遗传性血色病诊断中的作用。