"Autosomal recessive" 是指一种遗传方式，其中两个等位基因都是隐性基因（即它们是疾病或特征的基因），并且它们同时存在于一对染色体上，导致疾病或特征的出现。这种遗传方式通常涉及多个基因，并且通常在近亲结婚的人群中更常见。
以下是一篇关于“autosomal recessive”的英文范文：
Autosomal Recessive Genetic Diseases: Causes and Prevention
Autosomal recessive diseases are a type of genetic disorder that occurs when two recessive genes are inherited from both parents. These genes are usually located on the autosomes, which are chromosomes that do not determine sex characteristics.
The most common autosomal recessive diseases include cystic fibrosis, sickle cell anemia, and dwarfism. These diseases can be prevented by genetic testing and prenatal diagnosis, which can help identify individuals who are at risk of inheriting these diseases and provide appropriate treatment and support.
In addition, it is important to raise awareness about autosomal recessive diseases among the general public and healthcare professionals to ensure that individuals who are at risk of inheriting these diseases receive appropriate care and support.
"Autosomal recessive" 是遗传学中的一个术语，指的是一种基因遗传方式，其中两个等位基因都是隐性（即基因型为aa）时才会表现出疾病或特征。这种遗传方式通常涉及多个基因，并且通常在家族中传递。
以下是一篇相关的英文范文：
标题：Autosomal Recessive Disease in a Family with a New Mutation Identified
摘要：本文描述了一个家族中出现的常染色体隐性遗传疾病，并报告了一个新的突变。该疾病在家族中具有高度遗传倾向，并导致一系列症状。通过遗传分析，我们确定了该突变的位置，并提供了对该疾病的理解和预防策略。
正文：
1. Introduction
Autosomal recessive inheritance refers to a genetic pattern in which a disease or trait is expressed only when both copies of a gene (alleles) are of a particular type (i.e., aa). This type of inheritance involves multiple genes and is often seen in complex diseases or traits.
2. Case Description
A family with a history of a particular autosomal recessive disease was identified. The disease was characterized by a series of symptoms, including developmental delay, intellectual disability, seizures, and other neurological abnormalities. The family had a high risk of passing down the disease, indicating an important role for genetic analysis in disease prevention and management.
3. Genetic Analysis
A new mutation was identified in the family using genetic analysis techniques. The mutation was located in a gene that was known to be involved in the development of the nervous system. This finding provided valuable insights into the pathogenesis of the disease and provided a basis for developing potential treatment strategies.
4. Conclusion
Autosomal recessive inheritance plays an important role in the development of complex diseases and traits. Genetic analysis can provide valuable insights into the pathogenesis of these diseases and help families identify potential risk factors for passing down the disease. In this case, a new mutation was identified that provided valuable information for understanding and preventing the disease in future generations.
“autosomal recessive”的意思是染色体隐性遗传。它是一种遗传学术语，指的是在遗传学中，如果一个基因的纯合子状态是有害的或致命的，那么这种基因的突变形式就是一种隐性遗传方式。
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