Sherman Stephanie L, Allen Emily G, Bean Lora H, Freeman Sallie B
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Ment Retard Dev Disabil Res Rev. 2007;13(3):221-7. doi: 10.1002/mrdd.20157.
Down syndrome (DS) is the most commonly identified genetic form of mental retardation and the leading cause of specific birth defects and medical conditions. Traditional epidemiological studies to determine the prevalence, cause, and clinical significance of the syndrome have been conducted over the last 100 years. DS has been estimated to occur in approximately 1 in 732 infants in the United States, although there is some evidence that variability in prevalence of estimates exist among racial/ethnic groups. Progress has been made in characterizing the specific types of chromosome errors that lead to DS and in identifying associated factors that increase the risk of chromosome 21 malsegregation, i.e., advanced maternal age and recombination. Studies to examine the variability of the presence of specific DS-associated birth defects and medical conditions provide evidence for genetic and environmental modifiers. Here, we provide a brief survey of studies that address the current state of the field and suggest gaps in research that can soon be filled with new multidisciplinary approaches and technological advances.
唐氏综合征(DS)是最常见的遗传性智力障碍形式,也是特定出生缺陷和病症的主要原因。在过去100年里,人们开展了传统流行病学研究来确定该综合征的患病率、病因及临床意义。据估计,美国每732名婴儿中约有1名患有唐氏综合征,不过有证据表明不同种族/族裔群体的患病率估计存在差异。在确定导致唐氏综合征的特定染色体错误类型以及识别增加21号染色体错误分离风险的相关因素(即高龄产妇和重组)方面已取得进展。研究特定唐氏综合征相关出生缺陷和病症存在情况的变异性,为基因和环境修饰因子提供了证据。在此,我们简要综述了阐述该领域现状的研究,并指出研究中的差距,这些差距很快就能通过新的多学科方法和技术进步得以填补。