hemophiliac
简明释义
英[ˌhiːməˈfɪlɪæk]美[ˌhiːməˈfɪliæk]
n. 血友病患者
adj. 血友病的
英英释义
A person who has hemophilia, a genetic disorder that impairs the body's ability to make blood clots. | 一个患有血友病的人,这是一种遗传性疾病,影响身体凝血的能力。 |
单词用法
一名血友病患者 | |
血友病症状 | |
与血友病共存 | |
血友病障碍 | |
治疗血友病患者 | |
血友病治疗 |
同义词
出血者 | The bleeder needs to be careful during sports to avoid injuries. | 出血者在运动时需要小心,以避免受伤。 | |
血友病患者 | 血友病患者必须携带医疗警报卡。 |
反义词
健康的 | 他是一个健康的人,没有任何医疗问题。 | ||
正常的 | 正常的血液凝固对整体健康至关重要。 |
例句
1.Because I was not hemophiliac, I was not at risk.
我并非非血友病患者,我以为我没有危险;
2.Because I was not hemophiliac, I was not at risk.
我并非非血友病患者,我以为我没有危险;
3.The doctor explained that being a hemophiliac 血友病患者 means that the patient has difficulty with blood clotting.
医生解释说,作为一个hemophiliac血友病患者意味着患者在凝血方面有困难。
4.Children who are hemophiliacs 血友病患者 need to be monitored closely during physical activities.
需要密切监测在体育活动中表现的儿童,他们是hemophiliacs血友病患者。
5.Research is ongoing to find better treatments for hemophiliacs 血友病患者 worldwide.
全球范围内正在进行研究,以寻找对hemophiliacs血友病患者更好的治疗方法。
6.A hemophiliac 血友病患者 must carry a medical alert bracelet in case of emergencies.
一个hemophiliac血友病患者在紧急情况下必须佩戴医疗警报手环。
7.Parents of hemophiliac 血友病患者 children often learn how to manage bleeding episodes at home.
血友病患者的父母通常会学习如何在家中处理出血事件。
作文
Hemophilia is a genetic disorder that affects the blood's ability to clot. Individuals who suffer from this condition are referred to as hemophiliacs (血友病患者). This means that even small injuries can lead to excessive bleeding, which can be life-threatening if not managed properly. The disorder is typically inherited and predominantly affects males, although females can be carriers of the gene. Understanding hemophilia is crucial for both those affected and society as a whole, as it highlights the importance of medical care and awareness.In many cases, hemophiliacs (血友病患者) may not realize they have the condition until they experience significant bleeding after an injury or surgery. This can be a frightening experience, leading to hospital visits and sometimes emergency procedures to stop the bleeding. For families with a history of hemophilia, it is essential to undergo genetic testing and counseling to understand the risks and implications of the disorder.The management of hemophilia involves regular treatment and monitoring. Many hemophiliacs (血友病患者) receive infusions of clotting factor concentrates, which help their blood to clot more effectively. This treatment can significantly improve the quality of life for those affected, allowing them to participate in activities that might otherwise pose a risk of injury. However, access to these treatments can vary widely depending on geographical location and healthcare systems.Awareness and education about hemophilia are vital. Many people still hold misconceptions about the disorder, believing that it only affects a small number of individuals or that it is a disease of the past. In reality, there are thousands of hemophiliacs (血友病患者) worldwide who require ongoing medical attention and support. Organizations dedicated to hemophilia advocacy work tirelessly to promote awareness and provide resources for patients and their families.Living with hemophilia can be challenging, but with proper care and support, hemophiliacs (血友病患者) can lead fulfilling lives. It is important for society to recognize the needs of these individuals and to ensure that they have access to the necessary medical treatments. Additionally, fostering understanding and empathy within communities can help reduce stigma and promote inclusion.In conclusion, hemophilia is a serious condition that affects many individuals globally. Understanding what it means to be a hemophiliac (血友病患者) is essential for providing the appropriate support and care. Through education, awareness, and advancements in medical treatment, we can improve the lives of those living with this disorder and help them thrive despite the challenges they face.
血友病是一种遗传性疾病,影响血液的凝固能力。患有这种疾病的人被称为血友病患者。这意味着即使是小伤也可能导致过度出血,如果不妥善处理,可能危及生命。该疾病通常是遗传的,主要影响男性,尽管女性也可能携带该基因。了解血友病对患者及整个社会都至关重要,因为它突显了医疗护理和意识的重要性。在许多情况下,血友病患者可能在经历重大出血后才意识到自己患有此病。这可能是一次令人恐惧的经历,导致医院就诊,有时甚至需要紧急手术来止血。对于有血友病家族史的家庭,进行基因检测和咨询以了解疾病的风险和影响至关重要。血友病的管理涉及定期治疗和监测。许多血友病患者接受凝血因子浓缩物的输注,这有助于他们的血液更有效地凝固。这种治疗可以显著改善受影响者的生活质量,使他们能够参与可能会造成伤害的活动。然而,获得这些治疗的机会因地理位置和医疗系统而异。提高对血友病的认识和教育至关重要。许多人仍然对这种疾病持有误解,认为它只影响少数人或是过去的疾病。实际上,全球有成千上万的血友病患者需要持续的医疗关注和支持。致力于血友病倡导的组织不懈努力,以促进意识并为患者及其家庭提供资源。与血友病共存可能具有挑战性,但通过适当的护理和支持,血友病患者可以过上充实的生活。社会认识到这些个体的需求,并确保他们能够获得必要的医疗治疗是重要的。此外,在社区内培养理解和同情心可以帮助减少污名化,并促进包容性。总之,血友病是一种严重的疾病,影响着全球许多人。理解成为一名血友病患者意味着什么,对于提供适当的支持和护理至关重要。通过教育、意识和医疗治疗的进步,我们可以改善那些生活在这种疾病中的人的生活,并帮助他们克服面临的挑战。