Don't get confused by internet searches. Down syndrome is a chromosomal disorder and the double marker test is done between 11-13 weeks to screen for it. Talk to your gynac clearly, they will explain the scan reports.
This is a genetic condition caused by an extra chromosome. I know how stressful it is to wait for the screening results, especially after going through IVF. Just take a deep breath, these tests are standard and we are all here for you.
It's a genetic condition where baby has an extra chromosome, affecting their development. Doctors check for this through the NT scan and double marker blood test in the first trimester. It's a routine screening we all go through.
Oh sweetie, reading about Down syndrome can be so overwhelming. I remember crying before my NT scan out of pure fear. But please know these are just routine risk-assessment screenings that every pregnant woman gets.
Look, Down syndrome is a chromosomal condition. In pregnancy, doctors do screenings like NT scan and NIPT to check the risk level. If reports are normal, there's nothing to worry about.
Behan, ye ek genetic cheez hoti hai jisme bache ka vikas thoda alag hota hai. Doctor teesre mahine me blood test aur ultrasound se iska pata lagate hain. Apne doctor ki salah lo, sab theek hoga.
