Hook E B
Obstet Gynecol. 1981 Sep;58(3):282-5.
Estimates are made of the rates of all clinically significant cytogenetic abnormalities in live births by 1-year maternal age intervals ranging from 15 to 49. Down syndrome results from the most prevalent clinically significant cytogenetic abnormality, yet the rates of disorders associated with other cytogenetic abnormalities also increase with maternal age and significantly contribute to the overall rate at the older ages. The estimated rate of all clinically significant cytogenetic abnormalities rises from about 2 per 1000 (1 per 500) at the youngest maternal ages to about 2.6 per 1000 (1 per 270) at age 30, 5.6 per 1000 (1 per 80) at age 35, 15.8 per 1000 (1 per 60) at age 40, and 53.7 per 1000 (1 per 20) at age 45.
按母亲年龄1年间隔(范围从15岁至49岁)估算活产中所有具有临床意义的细胞遗传学异常发生率。唐氏综合征源于最常见的具有临床意义的细胞遗传学异常,但与其他细胞遗传学异常相关疾病的发生率也随母亲年龄增加而上升,且在较高年龄时对总体发生率有显著影响。所有具有临床意义的细胞遗传学异常的估计发生率,从最年轻母亲年龄时的约每1000例2例(每500例1例),上升至30岁时的约每1000例2.6例(每270例1例)、35岁时的每1000例5.6例(每80例1例)、40岁时的每1000例15.8例(每60例1例)以及45岁时的每1000例53.7例(每20例1例)。