heterotaxy

简明释义

英[ˈhetərəˌtæksi]美[ˈhetərəˌtæksi]

内脏异位

英英释义

单词用法

同义词

反义词

例句

1.Objective to analyse the risk factors for early mortality in patients with heterotaxy syndrome undergoing single ventricle series palliation.

目的分析单心室系列手术治疗内脏异位综合征早期死亡的危险因素。

2.Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy (situs ambiguous), such as cardiovascular anomalies.

完全性内脏逆位在50%原发性纤毛运动障碍患者中出现。有少数病例报道原发性纤毛运动障碍伴有内脏逆位，比如心血管畸形。

3.Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy (situs ambiguous), such as cardiovascular anomalies.

完全性内脏逆位在50%原发性纤毛运动障碍患者中出现。有少数病例报道原发性纤毛运动障碍伴有内脏逆位，比如心血管畸形。

4.Heterotaxy There tended to be duplication of...

内脏异位(倾象于左侧内脏结构重复)。

5.Research on heterotaxy has revealed various genetic factors that contribute to this condition, known as 异位性.

对异位性的研究揭示了多种遗传因素，这些因素导致了这一状况。

6.Doctors often conduct imaging studies to diagnose heterotaxy, or 异位性, in patients presenting with congenital heart defects.

医生通常会进行影像学研究，以诊断出现先天性心脏缺陷的患者是否患有异位性。

7.Children with heterotaxy may face numerous health challenges, including issues related to their 异位性 organ placement.

患有异位性的儿童可能面临许多健康挑战，包括与他们的器官位置相关的问题。

8.The surgical management of heterotaxy involves a multidisciplinary team due to its complexity and the need for 异位性 care.

由于其复杂性和对异位性护理的需求，异位性的外科管理涉及多学科团队。

9.In patients with heterotaxy, or 异位性, the arrangement of internal organs can be significantly different from the typical configuration.

在患有异位性的患者中，内脏器官的排列可能与典型配置有显著不同。

作文

Heterotaxy is a fascinating biological phenomenon that refers to the abnormal arrangement of organs or structures in the body. This condition can lead to a variety of health issues, depending on which organs are affected and how they are positioned. In the study of developmental biology, understanding heterotaxy (异位症) is crucial for unraveling the complexities of organ development and function. The term heterotaxy (异位症) is derived from the Greek words 'hetero,' meaning different, and 'taxis,' meaning arrangement. In normal human anatomy, organs are arranged in a specific manner; for example, the heart is located on the left side of the chest. However, in individuals with heterotaxy (异位症), this arrangement can be disrupted, leading to a mirror-image placement of organs or other atypical configurations. This condition can affect various organs, including the heart, lungs, and digestive system, often resulting in serious medical complications.One of the most critical aspects of heterotaxy (异位症) is its impact on the cardiovascular system. In many cases, individuals with this condition may have congenital heart defects, which can complicate their overall health and require surgical intervention. For instance, in cases of situs inversus, a type of heterotaxy (异位症), the heart is located on the right side of the chest instead of the left. While some people with situs inversus may not experience significant health problems, others may face severe complications due to associated heart defects.Research into heterotaxy (异位症) has revealed that genetic factors play a significant role in its occurrence. Certain gene mutations can disrupt the normal signaling pathways involved in organ positioning during embryonic development. Scientists continue to explore these genetic links to better understand how heterotaxy (异位症) develops and to identify potential therapeutic targets for treatment.In addition to its biological significance, heterotaxy (异位症) also raises intriguing questions about the nature of human anatomy and variation. The study of such anomalies challenges our understanding of what constitutes 'normal' anatomy and encourages a broader perspective on human diversity. By examining cases of heterotaxy (异位症), researchers can gain insights into the intricate processes that govern organ development and the remarkable adaptability of the human body.Furthermore, the implications of heterotaxy (异位症) extend beyond individual health. Understanding this condition can inform public health strategies and improve clinical practices for managing congenital anomalies. As medical technology advances, early detection and intervention for individuals with heterotaxy (异位症) may become more feasible, leading to better health outcomes and quality of life for those affected.In conclusion, heterotaxy (异位症) is a complex and multifaceted condition that offers valuable insights into human anatomy, genetics, and developmental biology. As we continue to study this phenomenon, we enhance our understanding of the human body and pave the way for improved medical care for individuals with this condition. The exploration of heterotaxy (异位症) not only enriches our knowledge of biology but also highlights the importance of embracing diversity in human health and development.

异位症是一个引人入胜的生物现象，指的是身体器官或结构的异常排列。这种情况可能导致各种健康问题，具体取决于受影响的器官以及它们的位置。在发育生物学研究中，理解异位症对于揭开器官发育和功能的复杂性至关重要。 异位症一词源自希腊语中的“hetero”，意为不同，以及“taxis”，意为排列。在正常的人体解剖中，器官以特定的方式排列；例如，心脏位于胸部的左侧。然而，在患有异位症的个体中，这种排列可能会被打乱，导致器官的镜像放置或其他非典型配置。这种情况可能影响各种器官，包括心脏、肺和消化系统，通常会导致严重的医学并发症。异位症的一个关键方面是其对心血管系统的影响。在许多情况下，患有这种疾病的个体可能有先天性心脏缺陷，这可能使他们的整体健康复杂化，并需要外科干预。例如，在一种叫做内脏反转的情况下，心脏位于胸部的右侧而不是左侧。虽然一些患有内脏反转的人可能不会经历显著的健康问题，但由于相关的心脏缺陷，其他人可能面临严重的并发症。对异位症的研究表明，遗传因素在其发生中起着重要作用。某些基因突变可能会干扰胚胎发育过程中器官定位的正常信号通路。科学家们继续探索这些遗传联系，以更好地理解异位症的发展，并识别潜在的治疗靶点。除了生物学意义外，异位症还引发了关于人体解剖和变异本质的有趣问题。这种异常的研究挑战了我们对“正常”解剖的理解，并鼓励我们对人类多样性采取更广泛的视角。通过检查异位症的案例，研究人员可以获得有关控制器官发育的复杂过程以及人类身体惊人适应能力的洞察。此外，异位症的影响超越了个体健康。理解这种情况可以为公共健康战略提供信息，并改善管理先天性异常的临床实践。随着医疗技术的进步，早期检测和干预患有异位症的个体可能变得更加可行，从而改善这些人的健康结果和生活质量。总之，异位症是一个复杂且多面的疾病，为我们提供了有关人类解剖、遗传学和发育生物学的宝贵见解。随着我们继续研究这一现象，我们增强了对人体的理解，并为改善患有此病个体的医疗护理铺平了道路。对异位症的探索不仅丰富了我们对生物学的知识，而且突显了拥抱人类健康和发展的多样性的重要性。