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新生儿血红蛋白病筛查:超出目标的益处。

Newborn screening for hemoglobinopathies: the benefit beyond the target.

作者信息

Grover R, Newman S, Wethers D, Anyane-Yeboa K, Pass K

出版信息

Am J Public Health. 1986 Oct;76(10):1236-7. doi: 10.2105/ajph.76.10.1236.

Abstract

As a result of New York State's Newborn Screening Program 4,565 neonates with trait hemoglobinopathies were identified and 3,200 families were notified of the results of testing their infants in New York City in 1982. Of the 1,531 families (2,190 parents) tested and counseled, 22 parents were diagnosed with sickle cell disease and 39 couples were found to be at-risk for having a child with sickle cell disease. Amniocentesis was performed in 14 of the 28 at-risk pregnant women and three of the four affected pregnancies were terminated. MCH-331001-01 to 04

摘要

由于纽约州新生儿筛查项目,1982年在纽约市共识别出4565名患有血红蛋白病特征的新生儿,并将检测结果通知了3200个家庭。在接受检测和咨询的1531个家庭(2190名父母)中,22名父母被诊断患有镰状细胞病,39对夫妇被发现有生育患镰状细胞病孩子的风险。28名有风险的孕妇中有14名接受了羊水穿刺检查,4例受影响的妊娠中有3例终止妊娠。MCH - 331001 - 01至04

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Newborn screening: a potpourri of policies.新生儿筛查:政策杂烩。
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Neonatal screening of sickle cell anemia: a preliminary report.新生儿镰状细胞贫血筛查:初步报告。
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Newborn screening: a potpourri of policies.新生儿筛查:政策杂烩。
Am J Public Health. 1986 Oct;76(10):1191-2. doi: 10.2105/ajph.76.10.1191.

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Genetic screening: implications for preventive medicine.基因筛查:对预防医学的影响。
Am J Public Health. 1983 Mar;73(3):243-5. doi: 10.2105/ajph.73.3.243.
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Prenatal diagnosis of hemoglobinopathies.血红蛋白病的产前诊断。
Pediatr Clin North Am. 1978 Aug;25(3):631-42. doi: 10.1016/s0031-3955(16)33608-2.

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