2011
DOI: 10.1007/s00404-011-2175-4
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Ultrasound evaluation of the fetal nasal bone: what is the most appropriate first-trimester cut-off point for aneuploidy screening?

Abstract: The best tool for aneuploidy screening was the qualitative NB test (absent vs. present). Ultrasonography of the NB is a component of aneuploidy screening, and should not be used alone.

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Cited by 4 publications
(4 citation statements)
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“…To date, in the first trimester, only the absence of NB has been consistently demonstrated to increase the risk of trisomy 21, whereas the clinical implications of NB hypoplasia have not been fully elucidated. In two independent studies, the presence of NB hypoplasia (length below the 10th centile) in the first trimester has not been found to correlate with the risk of aneuploidies as demonstrated in the second trimester . Conversely, other studies have shown a correlation between the sonographic demonstration of a hypoplastic NB in the first trimester and the risk of trisomy 21 .…”
Section: Discussionmentioning
confidence: 94%
“…To date, in the first trimester, only the absence of NB has been consistently demonstrated to increase the risk of trisomy 21, whereas the clinical implications of NB hypoplasia have not been fully elucidated. In two independent studies, the presence of NB hypoplasia (length below the 10th centile) in the first trimester has not been found to correlate with the risk of aneuploidies as demonstrated in the second trimester . Conversely, other studies have shown a correlation between the sonographic demonstration of a hypoplastic NB in the first trimester and the risk of trisomy 21 .…”
Section: Discussionmentioning
confidence: 94%
“…Previously, first-trimester screening test parameters including nuchal translucency, serum fβ-hCG, PAPP-A and ductus venosus were investigated for their associations with adverse perinatal outcomes (1,2,4,5,11). NB is one of the additional parameters of the first-trimester screening test and usually its absence or hypoplasia is found to be associated with chromosomal abnormalities (6,12). However, the possible association of NBL and the adverse perinatal outcome has not yet been assessed.…”
Section: Discussionmentioning
confidence: 99%
“…35 A small nose is a common facial feature of individuals with trisomy 21. 36 First-trimester nasal bone length has been proposed to be a component of aneuploidy screening. 37 Further, in 62.1% of fetuses with trisomy 21, the nasal bones were divergent, whereas in 131 of 135 (97.0%) euploid fetuses, the bones were entirely fused in the midline.…”
Section: Imaging Of the Profilementioning
confidence: 99%