How to detect chromosomal abnormalities in pregnancy?
My doc mentioned some tests for this and honestly i didnt fully understand. Im 11 weeks and thoda darr lag raha hai because of family history. Can someone explain what tests are usually done and when?
I completely understand the anxiety around these tests, it can be so scary to think about. But please take a deep breath; doctors do these standard tests just to be safe. It is usually done through blood tests and specific ultrasounds.
Chromosomal abnormalities are screened using the NT Scan and Double Marker test between weeks 11 and 13. If there is a high risk, doctors recommend advanced tests like NIPT (Non-Invasive Prenatal Testing) or Amniocentesis. Always follow your gynecologist's advice on which tests are necessary for your age and history.
These chromosomal screenings like NIPT can be quite expensive in private clinics. You can ask your doctor if the basic NT scan and Double Marker test are sufficient first, as they are cheaper and widely available. Planning these expenses early helps a lot.
These tests are so important for peace of mind, dear. I went through the NT scan and double marker test in my first trimester, and everything came out normal. It's just a simple blood test and a detailed scan, so try not to stress.
I felt so nervous during my 12th-week scan where they check the baby's neck thickness (NT scan). My doctor also recommended the double marker blood test. Doing these at the right week is very important, so consult your gynac soon.
