hemophilia

简明释义

英[ˌhiːməˈfɪliə]美[ˌhiːməˈfɪliə]

n. [内科]血友病（等于 haemophilia）

英英释义

单词用法

同义词

反义词

例句

1.Objective To find out a simple and specific method for genetic diagnosis of hemophilia a and identification of carriers.

目的探索一种更简便和更特异的方法，用于血友病a的基因诊断及其家系遗传咨询。

2.Researchers have long dreamed of treating diseases from hemophilia to cancer by replacing mutant genes with normal ones.

研究人员长期以来一直梦想用正常基因取代突变基因的方法治疗血友病，癌症等各种疾病。

3.As genetic blood disorders, hemophilia and porphyria had serious effects on the crowned heads of Europe.

血友病和卟啉病这两种遗传性血液病，在欧洲的皇室内产生了严重的影响。

4.Hemophilia was first described in 1803.

血友病在1803年初次被描述。

5.Objective To improve the physician' s understand of acquired hemophilia (AH) , and discuss optimal therapy schemes of AH.

目的提高对获得性血友病（AH）的认识，探讨其最佳治疗方案。

6.The family apparently suffered from a very rare form of hemophilia, indeed.

这一家族似乎真的罹患一种罕见的血友病。

7.The aim of this study was to investigate the efficacy of hepatocyte transplantation in the mouse model of hemophilia B.

该研究的目的在于研究肝细胞移植在小鼠B型血友病模型中的效果。

8.Hemophilia can be mild, moderate, or severe, depending on how much clotting factor is present in one's blood.

血友病可以是轻微、温和的，或者是剧烈的，这是根据人体血液里凝血因子的多少而定。

9.Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.

血友病：一种遗传性出血性疾病，因先天性缺乏某种凝血因子而引起。

10.The doctor explained that hemophilia 血友病 is a genetic disorder that affects blood clotting.

医生解释说，hemophilia 血友病 是一种影响血液凝固的遗传疾病。

11.Awareness campaigns about hemophilia 血友病 help educate the public on its symptoms and treatments.

关于hemophilia 血友病 的宣传活动帮助公众了解其症状和治疗方法。

12.People with hemophilia 血友病 may require clotting factor replacement therapy.

患有hemophilia 血友病的人可能需要进行凝血因子替代治疗。

13.Regular check-ups are essential for managing hemophilia 血友病 effectively.

定期检查对于有效管理hemophilia 血友病至关重要。

14.Children with hemophilia 血友病 often have to avoid certain sports to prevent injuries.

患有hemophilia 血友病 的儿童通常需要避免某些运动以防止受伤。

作文

Hemophilia is a genetic disorder that affects the blood's ability to clot, leading to excessive bleeding even from minor injuries. People with this condition often live in fear of bleeding episodes, which can be life-threatening if not managed properly. The disorder is primarily inherited and is more common in males than females due to its linkage to the X chromosome. Understanding hemophilia (血友病) is crucial for both patients and their families, as it impacts not only the individual but also their loved ones. The symptoms of hemophilia (血友病) can vary in severity depending on the level of clotting factors present in the blood. Individuals with severe hemophilia (血友病) may experience spontaneous bleeding without any apparent cause, while those with mild forms of the disorder might only bleed excessively during surgeries or after injuries. Common sites of bleeding include joints, muscles, and internal organs, making it essential for individuals with hemophilia (血友病) to be vigilant about their health. Treatment for hemophilia (血友病) typically involves replacement therapy, where the missing clotting factors are infused into the bloodstream. This treatment can help prevent bleeding episodes and manage the condition effectively. In recent years, advancements in gene therapy have shown promise in providing long-term solutions for individuals with hemophilia (血友病), potentially reducing or eliminating the need for regular infusions. Living with hemophilia (血友病) requires a proactive approach to health management. Patients must work closely with healthcare providers to monitor their condition and develop personalized treatment plans. Education plays a vital role in managing hemophilia (血友病), as understanding the disorder empowers individuals to make informed decisions about their care. Support groups and organizations dedicated to hemophilia (血友病) can provide valuable resources and a sense of community for those affected by the disorder. Moreover, raising awareness about hemophilia (血友病) is essential for fostering understanding and support within society. Many people are unaware of the challenges faced by individuals with this condition, and increasing public knowledge can lead to better support systems and resources. Schools, workplaces, and communities should be educated about hemophilia (血友病) to ensure that individuals living with the disorder can thrive without fear of discrimination or misunderstanding. In conclusion, hemophilia (血友病) is a complex disorder that requires comprehensive management and support. By understanding the nature of the condition and advocating for awareness, we can create a more inclusive environment for those affected by hemophilia (血友病). With ongoing research and advancements in treatment, there is hope for improved quality of life and outcomes for individuals living with this challenging disorder.

血友病是一种遗传性疾病，影响血液凝固的能力，导致即使是轻微的伤害也会出现过度出血。患有这种疾病的人常常生活在对出血事件的恐惧中，这可能在没有适当管理的情况下危及生命。这种疾病主要是遗传的，因其与X染色体的联系而在男性中更为常见。理解血友病对患者及其家庭至关重要，因为它不仅影响个人，还影响他们的亲人。血友病的症状可能因血液中凝血因子的水平而异，严重程度不同。严重的血友病患者可能会毫无明显原因地经历自发性出血，而轻度患者可能只在手术或受伤后出现过度出血。常见的出血部位包括关节、肌肉和内脏，因此，患有血友病的人必须对自己的健康保持警惕。血友病的治疗通常涉及替代疗法，即将缺失的凝血因子注入血液中。这种治疗可以帮助预防出血事件，有效管理这种疾病。近年来，基因治疗的进展为患有血友病的人提供了长期解决方案的希望，可能减少或消除定期输注的需求。与血友病共存需要积极的健康管理方法。患者必须与医疗提供者密切合作，监测他们的病情并制定个性化的治疗计划。教育在管理血友病中发挥着至关重要的作用，因为了解这种疾病使个人能够对自己的护理做出明智的决策。专门针对血友病的支持小组和组织可以为受影响的人提供宝贵的资源和社区感。此外，提高对血友病的认识对于促进社会的理解和支持至关重要。许多人对患有这种疾病的人的挑战一无所知，增加公众知识可以导致更好的支持系统和资源。学校、工作场所和社区应接受关于血友病的教育，以确保生活在这种疾病下的人能够在没有歧视或误解的情况下蓬勃发展。总之，血友病是一种复杂的疾病，需要全面的管理和支持。通过理解这种疾病的性质并倡导提高意识，我们可以为那些受到血友病影响的人创造一个更加包容的环境。随着研究的不断进行和治疗的进步，生活在这个挑战性疾病中的个人的生活质量和结果有望得到改善。