hemochromatosis

简明释义

英[ˌheməˌkrəʊməˈtəʊsɪs]美[ˌheməˌkroʊməˈtoʊsɪs]

n. [皮肤] 血色沉着病

英英释义

单词用法

同义词

反义词

例句

1.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。

2.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。

3.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。

4.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。

5.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。

6.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。

7.Early diagnosis of hemochromatosis is crucial for effective treatment.

早期诊断血色病对有效治疗至关重要。

8.Patients with hemochromatosis often experience fatigue and joint pain.

患有血色病的患者常常感到疲劳和关节疼痛。

9.Excess iron accumulation in the body leads to hemochromatosis.

体内铁的过量积累会导致血色病。

10.Genetic testing can determine if someone is at risk for hemochromatosis.

基因检测可以确定某人是否有患血色病的风险。

11.Dietary changes may help manage symptoms of hemochromatosis.

饮食改变可能有助于管理血色病的症状。

作文

Hemochromatosis is a medical condition characterized by excessive accumulation of iron in the body. This disorder can lead to serious health issues if not diagnosed and treated promptly. Individuals with hemochromatosis (血色病) often experience symptoms such as fatigue, joint pain, and abdominal discomfort. The body usually regulates iron levels through dietary intake and absorption, but in patients with hemochromatosis (血色病), this regulation fails, resulting in iron overload.The primary cause of hemochromatosis (血色病) is genetic mutations that affect the proteins responsible for iron absorption. The most common form is hereditary hemochromatosis (血色病), which is inherited in an autosomal recessive manner. This means that both parents must carry the mutated gene for their child to be affected. Early detection is crucial, as untreated hemochromatosis (血色病) can lead to severe complications, including liver cirrhosis, diabetes, and heart disease.Diagnosis typically involves blood tests that measure serum ferritin and transferrin saturation levels. Elevated levels of these markers indicate iron overload, prompting further investigation through genetic testing or liver biopsy. Once diagnosed, treatment options for hemochromatosis (血色病) include regular phlebotomy sessions to reduce iron levels in the body. Patients may also be advised to avoid iron-rich foods and vitamin C supplements, as vitamin C increases iron absorption.Living with hemochromatosis (血色病) requires ongoing management and lifestyle adjustments. Regular monitoring of iron levels is essential to prevent complications. Many patients lead healthy lives with proper treatment and dietary modifications. It is important for individuals with a family history of hemochromatosis (血色病) to discuss genetic testing with their healthcare provider, as early intervention can significantly improve outcomes.In conclusion, hemochromatosis (血色病) is a serious but manageable condition that affects iron metabolism in the body. Awareness and education about this disorder are vital for early detection and treatment. By understanding the implications of hemochromatosis (血色病) and taking proactive measures, individuals can minimize the risks associated with iron overload and maintain a better quality of life.