Abstract
Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies. It is associated commonly with chromosomal abnormalities (10%–30%) and additional structural abnormalities (55%–58%). Trisomy 13 and 18 are most commonly associated with aneuploidies, which are also associated with umbilical cord cysts and mesomelia.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
