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Towards adequate national provision of genomic testing in pregnancy

Towards adequate national provision of genomic testing in pregnancy
争取在全国范围内提供充足的妊娠期基因组检测
批准号:
nhmrc : 1059993
负责人:
A/Pr Howard Slater
金额:
$34.37万
依托单位国家:
澳大利亚
项目类别:
Project Grants
财政年份:
2014
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

项目摘要

项目成果

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中文摘要
翻译
现在可以使用染色体微阵列提供有关未出生儿童的基因组信息,这有可能彻底改变澳大利亚的孕产妇保健,但目前仅用于高风险妊娠。很快,所有孕妇,绝大多数目前正在进行产前筛查的孕妇,将能够使用这种和其他基因组技术。我们将研究胎儿基因组检测的心理影响,并在此过程中评估服务规划的需求,以及澳大利亚潜在的法律和政策变化。
英文摘要
Genomic information about unborn children can now be provided using chromosomal microarrays which have the potential to revolutionize maternal care in Australia, but are currently only used in high risk pregnancies. Soon all pregnant women, the vast majority who currently have prenatal screening, will be able to access this and other genomic technologies. We will examine the psychological impact of fetal genomic testing and, in doing so, assess the need for service planning, as well as potential legal and policy changes in Australia.
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Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study
  • 批准号:
    nhmrc : GNT1103389
  • 项目类别:
    Project Grants
  • 资助金额:
    $76.99万
  • 财政年份:
    2016
  • 负责人:
    A/Pr Howard Slater
  • 依托单位:
Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study
  • 批准号:
    nhmrc : 1103389
  • 项目类别:
    Project Grants
  • 资助金额:
    $52.79万
  • 财政年份:
    2016
  • 负责人:
    A/Pr Howard Slater
  • 依托单位:
海外基金