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Article

Detection of sex chromosome abnormalities by nuchal translucency screening at 10–14 weeks

1 Jun 1998

Abstract excerpt

At 10-14 weeks of gestation more than 80 per cent of fetuses affected by trisomy 21 can be detected by a screening programme based on a combination of maternal age and fetal nuchal translucency thickness (NT). The screen positive group in such a programme also identifies fetuses with sex chromosome abnormalities. In this ongoing multicentre screening study, involving 61,972 singleton pregnancies, 53 cases of sex...

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PMID: 9664603
DOI: 10.1002/(sici)1097-0223(199806)18:6<581::aid-pd301>3.0.co;2-6

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Detection of sex chromosome abnormalities by nuchal translucency screening at 10–14 weeksPMID 9664603Read ↗

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UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Fetal Medicine Foundation First Trimester Screening Group.Semantic proximity Read ↗

Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestation.Semantic proximity Read ↗

Quality Requirements for the early Fetal Ultrasound Assessment at 11–13+6 Weeks of Gestation (DEGUM Levels II and III)Semantic proximity Read ↗

Increased nuchal translucency thickness and normal karyotype: time for parental reassuranceSemantic proximity Read ↗

Screening for trisomy 18 by fetal nuchal translucency and maternal serum free β -hCG and PAPP-A at 10-14 weeks of gestationSemantic proximity Read ↗

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Screening for trisomy 13 by fetal nuchal translucency and maternal serum free ?-hCG and PAPP-A at 10-14 weeks of gestationSemantic proximity Read ↗

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