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nuchal scan
A nuchal scan (NT Procedure) is a sonographic prenatal screening scan (ultrasound) to help identify higher chances for chromosomal conditions including Down syndrome in a fetus, particularly for older women who have higher risks of such pregnancies. Increased thickness measurements are also associated with congenital heart defect.〔("Relationship Between Nuchal Translucency Thickness and Prevalence of Major Cardiac Defects in Fetuses With Normal Karyotype", by Atzei, A; Gajewska, K; Huggon, I C.; Allan, L; Nicolaides, K H. Obstetrical and Gynecological Survey. January 2006. Volume 61, Issue 1, pages 8-10. )〕 The scan is carried out at 11–13+6 weeks pregnancy and assesses the quantity of fluid collecting within the nape of the fetal neck. There are two distinct measurements – the nuchal translucency, which is measured earlier in pregnancy at the end of the first trimester, and for which there is a lower threshold for increased diameter, and the nuchal fold, which is measured towards the end of the second trimester. Fetuses with Down syndrome tend to have an increased amount of fluid around the neck. The scan may also help confirm both the accuracy of the pregnancy dates and the fetal viability. Its high definition imaging may also detect other less common chromosomal abnormalities. ==Indication== All women, whatever their age, have a small risk of delivering a baby with a physical or cognitive disability. The nuchal scan helps physicians estimate the risk of the fetus having Down syndrome or other abnormalities more accurately than by maternal age alone.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「nuchal scan」の詳細全文を読む
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