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唐氏综合征:产前风险评估与诊断

Down syndrome: prenatal risk assessment and diagnosis.

作者信息

Newberger D S

机构信息

State University of New York at Buffalo, USA.

出版信息

Am Fam Physician. 2000 Aug 15;62(4):825-32, 837-8.

Abstract

Down syndrome (trisomy 21) is the most commonly recognized genetic cause of mental retardation. The risk of trisomy 21 is directly related to maternal age. All forms of prenatal testing for Down syndrome must be voluntary. A nondirective approach should be used when presenting patients with options for prenatal screening and diagnostic testing. Patients who will be 35 years or older on their due date should be offered chorionic villus sampling or second-trimester amniocentesis. Women younger than 35 years should be offered maternal serum screening at 16 to 18 weeks of gestation. The maternal serum markers used to screen for trisomy 21 are alpha-fetoprotein, unconjugated estriol and human chorionic gonadotropin. The use of ultrasound to estimate gestational age improves the sensitivity and specificity of maternal serum screening.

摘要

唐氏综合征(21三体综合征)是最常见的公认的智力发育迟缓的遗传病因。21三体的风险与母亲年龄直接相关。所有形式的唐氏综合征产前检测都必须是自愿的。在向患者提供产前筛查和诊断检测选项时,应采用非指导性方法。预产期时年龄在35岁及以上的患者应接受绒毛取样或孕中期羊膜穿刺术。35岁以下的女性应在妊娠16至18周时接受母血清筛查。用于筛查21三体的母血清标志物是甲胎蛋白、未结合雌三醇和人绒毛膜促性腺激素。使用超声估计孕周可提高母血清筛查的敏感性和特异性。

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