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瑞典的产前诊断:组织与当前问题

Prenatal diagnosis in Sweden: organisation and current issues.

作者信息

Bui T H, Kristoffersson U

机构信息

Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.

出版信息

Eur J Hum Genet. 1997;5 Suppl 1:70-6.

PMID:9101184
Abstract

Invasive prenatal diagnosis was introduced in Sweden in the early 1970s and is an integral part of the public health care system. Funding is provided by taxation; the patient only pays a consultation fee. Genetic analyses on a broad range of cytogenetic and molecular disorders are performed at the 6 university-affiliated hospitals and in 1 county hospital. About 6% of all newborns have been cytogenetically screened during pregnancy, and about 90% of the analyses are performed after amniocentesis. The main indication is chromosome analysis because of advanced maternal age.

摘要

侵入性产前诊断于20世纪70年代初在瑞典引入,是公共医疗保健系统的一个组成部分。资金由税收提供;患者只需支付会诊费。6家大学附属医院和1家县医院对广泛的细胞遗传学和分子疾病进行基因分析。在孕期,约6%的新生儿接受了细胞遗传学筛查,其中约90%的分析是在羊膜穿刺术后进行的。主要指征是因产妇年龄偏大而进行染色体分析。

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