trisomic

简明释义

英[traɪˈsəʊmɪk]美[traɪˈsoʊmɪk]

adj. 三染色体的；一套半染色体的

英英释义

单词用法

同义词

反义词

例句

1.The gene controlling pubescence color(t)could be located on the extrachromosome of the new trisomic.

控制茸毛色的基因（t）可以定位在新三体的超数染色体上。

2.In the double trisomic 3, 6, six hybridization sites were detected.

在3号，6号染色体双三体上共有6个杂交位点。

3.Primary trisomic in barley played the important role in genetic and breeding.

大麦的初级三体在遗传育种上有重要价值。

4.The gene controlling pubescence color(t)could be located on the extrachromosome of the new trisomic.

控制茸毛色的基因（t）可以定位在新三体的超数染色体上。

5.In some cases, trisomic 三体症 individuals may have unique talents or abilities.

在某些情况下，trisomic 三体症个体可能具有独特的才能或能力。

6.Parents of a trisomic 三体症 child often seek support groups for guidance.

一个trisomic 三体症孩子的父母通常会寻求支持小组以获得指导。

7.The trisomic 三体症 condition can lead to various physical and developmental challenges.

这种trisomic 三体症状况可能导致各种身体和发育上的挑战。

8.The research focused on individuals with trisomic 三体症 conditions to understand their cognitive abilities.

这项研究集中在具有trisomic 三体症状况的个体，以了解他们的认知能力。

9.Doctors often encounter patients who are trisomic 三体症 during genetic screenings.

医生在基因筛查中经常遇到患有trisomic 三体症的患者。

作文

Trisomy is a genetic condition that occurs when an individual has three copies of a particular chromosome instead of the usual two. This can lead to various developmental and health issues, depending on which chromosome is affected. The most well-known example of a trisomic (三体性) condition is Down syndrome, which results from an extra copy of chromosome 21. Individuals with Down syndrome often face challenges related to cognitive development, physical growth, and increased susceptibility to certain health problems. Understanding trisomic (三体性) conditions is crucial for both medical professionals and families. Early diagnosis through genetic testing can provide valuable information about the potential challenges that a child may face. For instance, prenatal screening can identify the likelihood of a fetus being trisomic (三体性), allowing parents to make informed decisions regarding their pregnancy. Moreover, the impact of a trisomic (三体性) condition extends beyond the individual. Families often need to adapt their lifestyles to accommodate the unique needs of a trisomic (三体性) child. This may involve special educational programs, therapy sessions, and ongoing medical care. Support groups can also play a vital role in helping families navigate the complexities associated with raising a child who has a trisomic (三体性) condition. As society becomes more aware of genetic disorders, there is a growing emphasis on inclusion and support for individuals with trisomic (三体性) conditions. Schools and workplaces are increasingly adopting policies that promote diversity and accommodate the needs of those affected. This shift towards acceptance is essential, as it helps to combat stigma and fosters a more inclusive environment for everyone. Research continues to advance our understanding of trisomic (三体性) conditions. Scientists are exploring potential treatments and interventions that could improve the quality of life for individuals with these genetic anomalies. For example, therapies aimed at enhancing cognitive function or alleviating specific health issues are being investigated. The hope is that with continued research, we can uncover new ways to support those living with trisomic (三体性) conditions and help them lead fulfilling lives. In conclusion, trisomic (三体性) conditions represent a significant area of study within genetics and medicine. By promoting awareness and understanding, we can create a supportive environment for individuals and families affected by these conditions. As we continue to learn more about the complexities of genetic disorders, it is essential to advocate for inclusivity, research, and education to ensure that everyone has the opportunity to thrive, regardless of their genetic makeup.

三体性是一种遗传病，发生在个体的特定染色体上有三个拷贝而不是通常的两个。这可能导致各种发育和健康问题，具体取决于受影响的染色体。最著名的例子是唐氏综合症，它是由于21号染色体的额外拷贝引起的。患有唐氏综合症的个体通常面临与认知发展、身体生长以及对某些健康问题的易感性相关的挑战。理解trisomic（三体性）疾病对医疗专业人员和家庭至关重要。通过基因检测进行早期诊断可以提供有关孩子可能面临的潜在挑战的宝贵信息。例如，产前筛查可以识别胎儿成为trisomic（三体性）的可能性，使父母能够就怀孕做出明智的决定。此外，trisomic（三体性）疾病的影响不仅限于个体。家庭往往需要调整生活方式，以适应trisomic（三体性）儿童的独特需求。这可能涉及特殊教育项目、治疗课程和持续的医疗护理。支持小组在帮助家庭应对与养育有trisomic（三体性）状况的儿童相关的复杂性方面也发挥着至关重要的作用。随着社会对遗传疾病的认识不断提高，越来越强调对有trisomic（三体性）疾病的个体的包容和支持。学校和工作场所越来越多地采用促进多样性和满足受影响者需求的政策。这种接受度的转变至关重要，因为它有助于消除污名，并为每个人创造一个更具包容性的环境。研究继续推动我们对trisomic（三体性）疾病的理解。科学家们正在探索可能改善有这些遗传异常的个体生活质量的潜在治疗和干预措施。例如，旨在增强认知功能或缓解特定健康问题的疗法正在被研究。希望随着研究的持续，我们能够发现新的方法来支持那些与trisomic（三体性）疾病共同生活的人，并帮助他们过上充实的生活。总之，trisomic（三体性）疾病代表了遗传学和医学研究中的一个重要领域。通过促进意识和理解，我们可以为受到这些疾病影响的个体和家庭创造一个支持性的环境。随着我们继续了解遗传疾病的复杂性，倡导包容、研究和教育至关重要，以确保每个人都有机会蓬勃发展，无论其遗传构成如何。