chromosomally and anatomically normal fetuses with increased first trimester nuchal translucency conceived by icsi

نویسندگان

maryam niknejadi department of reproductive imaging, reproductive biomedicine research center, royan institute for reproductive biomedicine (acecr), tehran, iran; department of reproductive imaging, reproductive biomedicine research center, royan institute for reproductive biomedicine (acecr), tehran, iran p. o. box: 19395-4644, tehran, iran. tel: +98-212356246

hadieh haghighi department of reproductive imaging, reproductive biomedicine research center, royan institute for reproductive biomedicine (acecr), tehran, iran

چکیده

nuchal translucency (nt) measurements in the first trimester screening between 11 and 14 weeks’ gestation are regarded as a clear marker for aneuploidies. the presence of a thickened nt, even if the karyotype is normal, can be associated with structural abnormalities. having an abnormal screening of nt, parents and physicians could face dilemma over abortion particularly in a case of ivf/icsi fetuses. measurement of the nt thickness combined with biochemical markers has a false-positive rate of 5%. hereby we present six cases of chromosomally normal fetuses with an increased nt thickness in the first trimester, a normal karyotype and normal follow-up scans, who had a good prognosis for a normal early childhood. this report may help increase the confidence of couples who are reluctant to terminate the pregnancy.

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منابع مشابه

Chromosomally and Anatomically Normal Fetuses With Increased First Trimester Nuchal Translucency Conceived by ICSI

Nuchal translucency (NT) measurements in the first trimester screening between 11 and 14 weeks' gestation are regarded as a clear marker for aneuploidies. The presence of a thickened NT, even if the karyotype is normal, can be associated with structural abnormalities. Having an abnormal screening of NT, parents and physicians could face dilemma over abortion particularly in a case of IVF/ICSI f...

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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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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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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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Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation.

Increased fetal nuchal translucency thickness at 10-14 weeks of gestation is a common phenotypic expression of fetal chromosomal defects, structural abnormalities and genetic syndromes. This study reports on the prevalence of structural abnormalities and genetic syndromes in 4116 chromosomally normal pregnancies with increased fetal nuchal translucency thickness and reviews the relevant literat...

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[Increased nuchal translucency with normal karyotype].

Nuchal translucency (NT) measurement in first trimester screening between 11 and 14 weeks' gestation has now been clearly identified as a marker for aneuploidies and in particular for trisomy 21. Even in the absence of aneuploidy increased fetal nuchal translucency has been shown to be a marker for fetal heart malformations and numerous other fetal defects and genetic syndromes when the measure...

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عنوان ژورنال:
iranian journal of radiology

جلد ۱۲، شماره ۲، صفحات ۰-۰

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