scholarly journals By how much does increased nuchal translucency increase the risk of adverse pregnancy outcome in chromosomally normal fetuses? A study of 16 260 fetuses derived from an unselected pregnant population

2007 ◽  
Vol 29 (2) ◽  
pp. 150-158 ◽  
Author(s):  
M. Westin ◽  
S. Saltvedt ◽  
H. Almström ◽  
C. Grunewald ◽  
L. Valentin
Author(s):  
Reema Kumar Bhatt ◽  
Pranjali Dwivedi ◽  
Anubhuti Rana

Nuchal translucency (NT) measurement between 11- and 14-weeks’ gestation is an established and consistently performing marker for chromosomal abnormalities, including trisomy 21. Even in the absence of aneuploidy in the event of normal conventional karyotyping or microarray analysis, increased NT is prognosticative of adverse pregnancy outcome, because it is associated with miscarriages, congenital heart defects, several fetal malformations, many genetic syndromes, skeletal dysplasia’s, intrauterine death; the majority of these structural anomalies are undetectable before birth. The parents should be reassured that in the absence of any abnormality detected the fetus will have a normal uneventful outcome and postnatal development when compared to the general population outcome.


2007 ◽  
Vol 62 (10) ◽  
pp. 647-648
Author(s):  
J Piazze ◽  
M M. Anceschi ◽  
A Cerekja ◽  
R La Torre ◽  
A Pala ◽  
...  

2014 ◽  
Vol 35 (1) ◽  
pp. 22-24 ◽  
Author(s):  
S. Pitkanen ◽  
P. Laitinen ◽  
A. Yla-Outinen ◽  
M. Heikkila ◽  
T. Honkasalo ◽  
...  

10.1002/pd.61 ◽  
2001 ◽  
Vol 21 (5) ◽  
pp. 403-408 ◽  
Author(s):  
Ron Maymon ◽  
Eli Dreazen ◽  
Ian Buckovsky ◽  
Zwi Weinraub ◽  
Arie Herman

2007 ◽  
Vol 98 (1) ◽  
pp. 5-9 ◽  
Author(s):  
J. Piazze ◽  
M.M. Anceschi ◽  
A. Cerekja ◽  
R. La Torre ◽  
A. Pala ◽  
...  

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