P31.06: Pregnancy outcomes of fetuses with enlarged nuchal translucency

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منابع مشابه

High macrosomia rate in healthy fetuses after enlarged nuchal translucency.

OBJECTIVE The aim of this study was to investigate the association of the first trimester screening variables nuchal translucency (NT), pregnancy associated plasma protein (PAPP-A), and free beta-human chorionic gonadotrophin (βhCG) and birth weight, with a focus on the prediction of macrosomia. METHODS The database of our Fetal Medicine Unit was searched for all singleton pregnancies, who un...

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Enlarged nuchal translucency in chromosomally normal fetuses: strong association with orofacial clefts.

OBJECTIVES The aim of this study was to investigate whether there is an association between enlarged nuchal translucency (NT) and orofacial clefts. METHODS The pregnancy outcome of women who underwent an NT measurement between January 2000 and November 2008 was reviewed. All orofacial clefts detected prenatally and postnatally in karyotypically normal fetuses/infants were reviewed and a disti...

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Nuchal translucency measurement in fetuses with spinal muscular atrophy.

OBJECTIVE Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder with a high carrier frequency in the general population. The severity of this disorder indicates the importance of early prenatal detection. In medical literature, there are a few published case reports of enlarged nuchal translucency (NT) measurement in association with a diagnosis of SMA in the fetus....

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Increased nuchal translucency in fetuses with a normal karyotype.

Sonographic assessment of nuchal translucency (NT) thickness has been recognized as an effective means of screening for trisomy 21 and other chromosomal abnormalities at 11–14 weeks of gestation. Up to 80% of aneuploid fetuses have increased NT, but this feature is also found in 5% of karyotypically normal fetuses at this stage of pregnancy (Snijders et al., 1998). As this screening test examin...

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Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester.

OBJECTIVES To study the outcome of chromosomally normal pregnancies with increased nuchal translucency at the 10-14-week scan. DESIGN Retrospective study of 1320 chromosomally normal singleton pregnancies with nuchal translucency of > or = 3.5 mm. In addition to fetal karyotyping these patients were managed with follow-up scans at 14-16 and 20-22 weeks, specialist fetal echocardiography and i...

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ژورنال

عنوان ژورنال: Ultrasound in Obstetrics and Gynecology

سال: 2007

ISSN: 0960-7692

DOI: 10.1002/uog.4776