Polani P E, Alberman E, Alexander B J, Benson P F, Berry A C, Blunt S, Daker M G, Fensom A H, Garrett D M, McGuire V M, Roberts J A, Seller M J, Singer J D
J Med Genet. 1979 Jun;16(3):166-75. doi: 10.1136/jmg.16.3.166.
The work of one Genetic Centre over 16 years, covering about 14 000 kinships, is described. The numbers registered in a year increased from an average of 477 in the early 1960s to 1612 in 1976/1977. The increase is largely, but not entirely, attributable to the advent of prenatal diagnosis, and an account is given of our experience with this. In 1916 patients who had a successful amniocentesis, results indicative of fetal abnormality were found in 4.3% and a balanced translocation was found in an additional 0.9%. Results indicative of fetal abnormality were found in 3.5% of mothers referred because of a maternal age of 40 or more, 3.9% referred because of a high risk of neural tube defect, and 19.3% referred because of a high risk of an inborn error of metabolism. A number of cases with difficult diagnostic problems are described.
本文描述了一个遗传中心16年来的工作,涵盖了约14000个亲属关系。每年登记的数量从20世纪60年代初的平均477例增加到1976/1977年的1612例。这种增长在很大程度上,但并非完全归因于产前诊断的出现,并介绍了我们在这方面的经验。在1916例成功进行羊膜穿刺术的患者中,4.3%的结果表明胎儿异常,另有0.9%发现平衡易位。因母亲年龄40岁及以上而转诊的母亲中,3.5%的结果表明胎儿异常;因神经管缺陷高危而转诊的母亲中,3.9%的结果表明胎儿异常;因先天性代谢缺陷高危而转诊的母亲中,19.3%的结果表明胎儿异常。文中描述了一些诊断难题的病例。