congenital hypoplasia
简明释义
腹内发育不全
英英释义
Congenital hypoplasia refers to a condition where an organ or tissue is underdeveloped due to insufficient cell production during fetal development. | 先天性发育不良是指由于胎儿发育期间细胞生成不足,导致某个器官或组织发育不全的情况。 |
例句
1.The doctor diagnosed the patient with congenital hypoplasia (先天性发育不全) of the left kidney.
医生诊断患者左肾存在congenital hypoplasia (先天性发育不全)。
2.Children with congenital hypoplasia (先天性发育不全) may require special educational support.
患有congenital hypoplasia (先天性发育不全)的儿童可能需要特别的教育支持。
3.Early intervention can improve outcomes for children with congenital hypoplasia (先天性发育不全).
早期干预可以改善患有congenital hypoplasia (先天性发育不全)儿童的结果。
4.The pediatrician explained that congenital hypoplasia (先天性发育不全) can affect various organs.
儿科医生解释说,congenital hypoplasia (先天性发育不全)可能影响多种器官。
5.The research focused on the genetic factors contributing to congenital hypoplasia (先天性发育不全).
这项研究集中于导致congenital hypoplasia (先天性发育不全)的遗传因素。
作文
Congenital conditions can have a profound impact on an individual's health and quality of life. One such condition is congenital hypoplasia, which refers to the underdevelopment or incomplete development of a particular organ or tissue that occurs during fetal development. This condition can affect various parts of the body, including the heart, lungs, teeth, and more. Understanding congenital hypoplasia is crucial for early diagnosis and intervention, as it can lead to significant health challenges later in life.The term 'congenital' indicates that the condition is present at birth, while 'hypoplasia' comes from the Greek words 'hypo' meaning under and 'plasia' meaning formation. Therefore, congenital hypoplasia literally translates to 'under-formation at birth.' This condition can arise due to a variety of factors, including genetic mutations, environmental influences, or maternal health issues during pregnancy. For instance, if a mother is exposed to certain toxins, infections, or nutritional deficiencies, these can hinder the normal development of the fetus, leading to congenital hypoplasia of various organs.The effects of congenital hypoplasia can vary widely depending on the specific organ or tissue affected. In some cases, individuals may experience mild symptoms that require minimal intervention. However, in more severe cases, congenital hypoplasia can result in serious health complications that necessitate ongoing medical treatment. For example, children born with congenital hypoplasia of the teeth may have fewer teeth than normal, which can affect their ability to chew and speak properly. Similarly, congenital hypoplasia of the heart can lead to congenital heart defects, which may require surgical intervention shortly after birth.Diagnosis of congenital hypoplasia typically involves a combination of physical examinations, imaging studies, and sometimes genetic testing. Early detection is essential, as it allows healthcare providers to develop a tailored treatment plan to address the specific needs of the patient. Treatment options may include surgery, medication, or supportive therapies aimed at improving functionality and quality of life.In addition to medical interventions, families of individuals with congenital hypoplasia often require emotional and psychological support. Coping with the challenges of a congenital condition can be overwhelming, and access to resources such as counseling and support groups can be invaluable. It is important for families to connect with others who are facing similar challenges, as this can provide a sense of community and understanding.In conclusion, congenital hypoplasia is a complex condition that highlights the importance of prenatal care and early intervention. By understanding the implications of this condition and advocating for proper medical support, we can help improve the outcomes for those affected by congenital hypoplasia. Continued research into the causes and treatments for congenital conditions will also play a vital role in enhancing our understanding and management of these health issues, ultimately leading to better quality of life for affected individuals.
先天性疾病对个人的健康和生活质量有深远的影响。其中一个这样的疾病是先天性发育不良,指的是在胎儿发育期间某个特定器官或组织的发育不足或不完全。这种情况可以影响身体的各个部分,包括心脏、肺部、牙齿等。理解先天性发育不良对于早期诊断和干预至关重要,因为它可能在以后的生活中导致重大健康挑战。“先天性”一词表示这种情况在出生时就存在,而“发育不良”源于希腊语单词“hypo”,意为不足,以及“plasia”,意为形成。因此,先天性发育不良字面意思是“出生时的发育不足”。这种情况可能由于多种因素引起,包括基因突变、环境影响或孕期母体健康问题。例如,如果母亲接触到某些毒素、感染或营养缺乏,这些都可能阻碍胎儿的正常发育,从而导致各种器官的先天性发育不良。先天性发育不良的影响因受影响的特定器官或组织而异。在某些情况下,个体可能会经历轻微症状,只需最小的干预。然而,在更严重的情况下,先天性发育不良可能导致严重的健康并发症,需要持续的医疗治疗。例如,出生时有先天性发育不良的牙齿的儿童可能比正常人少牙齿,这会影响他们正常咀嚼和说话的能力。同样,先天性发育不良的心脏可能导致先天性心脏缺陷,这可能需要在出生后不久进行手术干预。先天性发育不良的诊断通常涉及身体检查、影像学检查,有时还包括基因检测。早期发现至关重要,因为这使医疗提供者能够制定量身定制的治疗计划,以满足患者的特定需求。治疗选择可能包括手术、药物或旨在改善功能和生活质量的支持性疗法。除了医疗干预外,患有先天性发育不良的个体的家庭通常需要情感和心理支持。应对先天性疾病的挑战可能是压倒性的,获得心理咨询和支持小组等资源可能是无价的。家庭与面临类似挑战的其他人建立联系也很重要,因为这可以提供一种社区感和理解。总之,先天性发育不良是一个复杂的疾病,突显了产前护理和早期干预的重要性。通过了解这种疾病的影响并倡导适当的医疗支持,我们可以帮助改善受先天性发育不良影响者的结果。对先天性疾病的原因和治疗的持续研究也将在增强我们对这些健康问题的理解和管理方面发挥重要作用,最终提高受影响个体的生活质量。
相关单词