Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks

Objectives To investigate the potential value of choroid plexus cyst, intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel as markers of trisomy 21 at 11 + 0 to 13 + 6 weeks. Methods We examined three‐dimensional volumes from 228 fetuses with trisomy 21 and 797 chromosomally normal...

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Veröffentlicht in:Ultrasound in obstetrics & gynecology 2008-02, Vol.31 (2), p.132-135
Hauptverfasser: Dagklis, T., Plasencia, W., Maiz, N., Duarte, L., Nicolaides, K. H.
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container_issue 2
container_start_page 132
container_title Ultrasound in obstetrics & gynecology
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creator Dagklis, T.
Plasencia, W.
Maiz, N.
Duarte, L.
Nicolaides, K. H.
description Objectives To investigate the potential value of choroid plexus cyst, intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel as markers of trisomy 21 at 11 + 0 to 13 + 6 weeks. Methods We examined three‐dimensional volumes from 228 fetuses with trisomy 21 and 797 chromosomally normal fetuses at 11 + 0 to 13 + 6 weeks of gestation. We looked for choroid plexus cysts with a minimum diameter of 1.5 mm, intracardiac echogenic focus, hydronephrosis with a minimum anteroposterior diameter of the pelvis of 1.5 mm and hyperechogenic bowel. Results The prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel was significantly higher in trisomy 21 than in normal fetuses (9.6% vs. 1.5%, 17.1% vs. 5.3% and 11.4% vs. 2.4%, respectively). There was no significant difference between the two groups in the prevalence of choroid plexus cysts (7.5% vs. 5.0%). There were no significant differences in crown–rump length or nuchal translucency thickness in either chromosomally normal or trisomy 21 fetuses between those with and those without any one of the markers. Conclusions At 11 + 0 to 13 + 6 weeks the prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel is higher in trisomy 21 than in chromosomally normal fetuses. As there is no significant association between the presence of these markers and nuchal translucency thickness, they could be included in the assessment of risk to improve accuracy of screening. Copyright © 2007 ISUOG. Published by John Wiley & Sons, Ltd.
doi_str_mv 10.1002/uog.5224
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H.</creator><creatorcontrib>Dagklis, T. ; Plasencia, W. ; Maiz, N. ; Duarte, L. ; Nicolaides, K. H.</creatorcontrib><description>Objectives To investigate the potential value of choroid plexus cyst, intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel as markers of trisomy 21 at 11 + 0 to 13 + 6 weeks. Methods We examined three‐dimensional volumes from 228 fetuses with trisomy 21 and 797 chromosomally normal fetuses at 11 + 0 to 13 + 6 weeks of gestation. We looked for choroid plexus cysts with a minimum diameter of 1.5 mm, intracardiac echogenic focus, hydronephrosis with a minimum anteroposterior diameter of the pelvis of 1.5 mm and hyperechogenic bowel. Results The prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel was significantly higher in trisomy 21 than in normal fetuses (9.6% vs. 1.5%, 17.1% vs. 5.3% and 11.4% vs. 2.4%, respectively). There was no significant difference between the two groups in the prevalence of choroid plexus cysts (7.5% vs. 5.0%). There were no significant differences in crown–rump length or nuchal translucency thickness in either chromosomally normal or trisomy 21 fetuses between those with and those without any one of the markers. Conclusions At 11 + 0 to 13 + 6 weeks the prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel is higher in trisomy 21 than in chromosomally normal fetuses. As there is no significant association between the presence of these markers and nuchal translucency thickness, they could be included in the assessment of risk to improve accuracy of screening. Copyright © 2007 ISUOG. Published by John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 0960-7692</identifier><identifier>EISSN: 1469-0705</identifier><identifier>DOI: 10.1002/uog.5224</identifier><identifier>PMID: 18085527</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Adult ; Biological and medical sciences ; Brain Diseases - diagnostic imaging ; Brain Diseases - embryology ; cardiac echogenic focus ; Cardiomyopathies - diagnostic imaging ; Cardiomyopathies - embryology ; Choroid Plexus - diagnostic imaging ; Choroid Plexus - embryology ; choroid plexus cysts ; Chromosome aberrations ; Crown-Rump Length ; Cysts - diagnostic imaging ; Cysts - embryology ; Down Syndrome - diagnostic imaging ; echogenic bowel ; Female ; Fetal Diseases - diagnostic imaging ; first‐trimester screening ; Gynecology. Andrology. Obstetrics ; Humans ; hydronephrosis ; Hydronephrosis - diagnostic imaging ; Hydronephrosis - embryology ; Intestinal Diseases - diagnostic imaging ; Intestinal Diseases - embryology ; Kidneys ; Medical genetics ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Nuchal Translucency Measurement ; Predictive Value of Tests ; Pregnancy ; Pregnancy Trimester, First ; Pregnancy Trimester, Second ; trisomy 21 ; Ultrasonography, Prenatal ; Urinary system involvement in other diseases. Miscellaneous</subject><ispartof>Ultrasound in obstetrics &amp; gynecology, 2008-02, Vol.31 (2), p.132-135</ispartof><rights>Copyright © 2007 ISUOG. Published by John Wiley &amp; Sons, Ltd.</rights><rights>2008 INIST-CNRS</rights><rights>Copyright (c) 2007 ISUOG. 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H.</creatorcontrib><title>Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks</title><title>Ultrasound in obstetrics &amp; gynecology</title><addtitle>Ultrasound Obstet Gynecol</addtitle><description>Objectives To investigate the potential value of choroid plexus cyst, intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel as markers of trisomy 21 at 11 + 0 to 13 + 6 weeks. Methods We examined three‐dimensional volumes from 228 fetuses with trisomy 21 and 797 chromosomally normal fetuses at 11 + 0 to 13 + 6 weeks of gestation. We looked for choroid plexus cysts with a minimum diameter of 1.5 mm, intracardiac echogenic focus, hydronephrosis with a minimum anteroposterior diameter of the pelvis of 1.5 mm and hyperechogenic bowel. Results The prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel was significantly higher in trisomy 21 than in normal fetuses (9.6% vs. 1.5%, 17.1% vs. 5.3% and 11.4% vs. 2.4%, respectively). There was no significant difference between the two groups in the prevalence of choroid plexus cysts (7.5% vs. 5.0%). There were no significant differences in crown–rump length or nuchal translucency thickness in either chromosomally normal or trisomy 21 fetuses between those with and those without any one of the markers. Conclusions At 11 + 0 to 13 + 6 weeks the prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel is higher in trisomy 21 than in chromosomally normal fetuses. As there is no significant association between the presence of these markers and nuchal translucency thickness, they could be included in the assessment of risk to improve accuracy of screening. Copyright © 2007 ISUOG. Published by John Wiley &amp; Sons, Ltd.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Brain Diseases - diagnostic imaging</subject><subject>Brain Diseases - embryology</subject><subject>cardiac echogenic focus</subject><subject>Cardiomyopathies - diagnostic imaging</subject><subject>Cardiomyopathies - embryology</subject><subject>Choroid Plexus - diagnostic imaging</subject><subject>Choroid Plexus - embryology</subject><subject>choroid plexus cysts</subject><subject>Chromosome aberrations</subject><subject>Crown-Rump Length</subject><subject>Cysts - diagnostic imaging</subject><subject>Cysts - embryology</subject><subject>Down Syndrome - diagnostic imaging</subject><subject>echogenic bowel</subject><subject>Female</subject><subject>Fetal Diseases - diagnostic imaging</subject><subject>first‐trimester screening</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>hydronephrosis</subject><subject>Hydronephrosis - diagnostic imaging</subject><subject>Hydronephrosis - embryology</subject><subject>Intestinal Diseases - diagnostic imaging</subject><subject>Intestinal Diseases - embryology</subject><subject>Kidneys</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nuchal Translucency Measurement</subject><subject>Predictive Value of Tests</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, First</subject><subject>Pregnancy Trimester, Second</subject><subject>trisomy 21</subject><subject>Ultrasonography, Prenatal</subject><subject>Urinary system involvement in other diseases. 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H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4144-a6f16626798a4f3a86415227538e85e10dcfa2703fa7beb46939048b816e8b323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Brain Diseases - diagnostic imaging</topic><topic>Brain Diseases - embryology</topic><topic>cardiac echogenic focus</topic><topic>Cardiomyopathies - diagnostic imaging</topic><topic>Cardiomyopathies - embryology</topic><topic>Choroid Plexus - diagnostic imaging</topic><topic>Choroid Plexus - embryology</topic><topic>choroid plexus cysts</topic><topic>Chromosome aberrations</topic><topic>Crown-Rump Length</topic><topic>Cysts - diagnostic imaging</topic><topic>Cysts - embryology</topic><topic>Down Syndrome - diagnostic imaging</topic><topic>echogenic bowel</topic><topic>Female</topic><topic>Fetal Diseases - diagnostic imaging</topic><topic>first‐trimester screening</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>hydronephrosis</topic><topic>Hydronephrosis - diagnostic imaging</topic><topic>Hydronephrosis - embryology</topic><topic>Intestinal Diseases - diagnostic imaging</topic><topic>Intestinal Diseases - embryology</topic><topic>Kidneys</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nuchal Translucency Measurement</topic><topic>Predictive Value of Tests</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First</topic><topic>Pregnancy Trimester, Second</topic><topic>trisomy 21</topic><topic>Ultrasonography, Prenatal</topic><topic>Urinary system involvement in other diseases. 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H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks</atitle><jtitle>Ultrasound in obstetrics &amp; gynecology</jtitle><addtitle>Ultrasound Obstet Gynecol</addtitle><date>2008-02</date><risdate>2008</risdate><volume>31</volume><issue>2</issue><spage>132</spage><epage>135</epage><pages>132-135</pages><issn>0960-7692</issn><eissn>1469-0705</eissn><abstract>Objectives To investigate the potential value of choroid plexus cyst, intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel as markers of trisomy 21 at 11 + 0 to 13 + 6 weeks. Methods We examined three‐dimensional volumes from 228 fetuses with trisomy 21 and 797 chromosomally normal fetuses at 11 + 0 to 13 + 6 weeks of gestation. We looked for choroid plexus cysts with a minimum diameter of 1.5 mm, intracardiac echogenic focus, hydronephrosis with a minimum anteroposterior diameter of the pelvis of 1.5 mm and hyperechogenic bowel. Results The prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel was significantly higher in trisomy 21 than in normal fetuses (9.6% vs. 1.5%, 17.1% vs. 5.3% and 11.4% vs. 2.4%, respectively). There was no significant difference between the two groups in the prevalence of choroid plexus cysts (7.5% vs. 5.0%). There were no significant differences in crown–rump length or nuchal translucency thickness in either chromosomally normal or trisomy 21 fetuses between those with and those without any one of the markers. Conclusions At 11 + 0 to 13 + 6 weeks the prevalence of intracardiac echogenic focus, hydronephrosis and hyperechogenic bowel is higher in trisomy 21 than in chromosomally normal fetuses. As there is no significant association between the presence of these markers and nuchal translucency thickness, they could be included in the assessment of risk to improve accuracy of screening. Copyright © 2007 ISUOG. Published by John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>18085527</pmid><doi>10.1002/uog.5224</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biological and medical sciences
Brain Diseases - diagnostic imaging
Brain Diseases - embryology
cardiac echogenic focus
Cardiomyopathies - diagnostic imaging
Cardiomyopathies - embryology
Choroid Plexus - diagnostic imaging
Choroid Plexus - embryology
choroid plexus cysts
Chromosome aberrations
Crown-Rump Length
Cysts - diagnostic imaging
Cysts - embryology
Down Syndrome - diagnostic imaging
echogenic bowel
Female
Fetal Diseases - diagnostic imaging
first‐trimester screening
Gynecology. Andrology. Obstetrics
Humans
hydronephrosis
Hydronephrosis - diagnostic imaging
Hydronephrosis - embryology
Intestinal Diseases - diagnostic imaging
Intestinal Diseases - embryology
Kidneys
Medical genetics
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Nuchal Translucency Measurement
Predictive Value of Tests
Pregnancy
Pregnancy Trimester, First
Pregnancy Trimester, Second
trisomy 21
Ultrasonography, Prenatal
Urinary system involvement in other diseases. Miscellaneous
title Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks
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