Trisomy 18 Lusine Karapetyan Article Published: Dec 20, 2018 Russia Case report33-year-old (G2P1) was sent to our unit for second trimester scan. First trimester scan was done with NT-3,2 mm (above 95 percentile). Calculated risk for trisomy 18 was 1:105. Although parents refused karyotyping and opted for continuation of the pregnancy.Our scanning at 21 and 30 weeks of pregnancy revealed atrioventricular septal defect, choroid plexus cyst (at 21 weeks), mild micrognathia, umbilical cord pseudocysts, clenched fists and overlapping fingers and intrauterine growth restriction. After birth fetal Karyotyping revealed 47XX+18 21 weeks Images 1 and 2:Â shows omplete form of atrioventricular septal defect. Images 3 and 4:Â show choroid plexus cyst and wide cavum septi pellucidi. Images 5 and 6:Â show two umbilical arteries and clenched fist. 30 30 weeks Images 7-9:Â show fetal face with mild micrognathia and clenched fist with overlapping fingers. videos Videos 1-3: shows atrioventricular septal defect (type A according to the Rastelli). Sorry, your browser doesn't support embedded videos. Sorry, your browser doesn't support embedded videos. Image 10 and video 3:Â show dilated umbilical cord with Whartonâs jelly edema and pseudocysts. Sorry, your browser doesn't support embedded videos. Discussion Board Start a discussion about this article Add to Favorites Favorite