Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study [PDF]
Previous studies have shown that over 40% of babies with Down syndrome have a major cardiac anomaly and are more likely to have other major congenital anomalies.
Addor, Marie-Claude +29 more
core +1 more source
EP12.03: Comparison of pregnancy outcomes in fetuses with increased nuchal translucency according to the sonographic features [PDF]
M. Kim +4 more
openalex +1 more source
OBJECTIVE: We sought to determine the value of well defined screening method in predicting trisomy cases in our institution. STUDY DESIGN: Totally 300 amniocentesis cases were screened from prospectively collected database.
Tülay Tos +6 more
doaj
Risk assessment for fetal trisomy 21 based on nuchal translucency measurement and biochemical screening at 11-13 weeks [PDF]
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenScreening for fetal aneuploidy during the first trimester using fetal nuchal translucency measurement and maternal serum free ss-hCG (ss-human chorionic ...
Hildur Harðardóttir
core
First‐trimester screening for Down syndrome in France combining fetal nuchal translucency measurement and biochemical markers [PDF]
Françoise Müller +5 more
openalex +1 more source
Background It becomes important to detect chromosomal abnormalities prenatally and early in the pregnancy. The present thesis is aimed to assess the performance of prenatal screening tests for chromosomal abnormalities detection i.e., dual ...
S. Sailaja, Bindu Reddy Pamulapati,
doaj
Correlation Between Sagittal and Transverse Plane Fetal Nuchal Translucency Measurement
Objective: This study aimed to evaluate and compare nuchal translucency (NT) measurement between sagittal and transverse planes for aneuploidy screening.
Pananya Jomphansa +5 more
doaj +1 more source
Risk assessment for fetal aneuploidy after nuchal translucency measurement [PDF]
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenIn this article the focus is on the estimation of a likelihood ratio by using software which calculates the risk for trisomy 13, 18 and 21. It is based on the
Kristín Rut Haraldsdóttir
core
P10.21: Karyotype and outcome of 43 fetuses diagnosed in the first trimester with cystic hygroma in relation with nuchal translucency measurement [PDF]
R. Kharrat +3 more
openalex +1 more source

