If you're looking for information on noninvasive prenatal testing (NIPT), you're likely in the very first trimester of maternity. Congrats! Take a deep breath and appreciate just how far you've already come. While this moment brings both pleasure and excitement, we know these early days can also spark anxieties when your OB-GYN or midwife begins discussing hereditary screening.
We understand that these decisions on your journey to parent can be difficult. But one means to feel more confident is to be well notified. We'll aid you navigate what the NIPT screening examination is, in addition to what it can (and also can't) tell you so you'll really feel more equipped to make the most effective selection for you.
By 10 weeks of maternity, your medical care service provider may speak to you concerning this elective examination as an alternative to assist identify if your baby goes to danger for hereditary irregularities, such as chromosomal disorders. Most generally, the test identifies the threat of disorders such as Down disorder (trisomy 21), Edwards disorder (trisomy 18), and Patau disorder (trisomy 13), as well as conditions brought on by missing or added X and Y chromosomes.
It's important to know that NIPT is a screening test not a diagnostic test. It can, however, predict whether the risk of a genetic problem is high or reduced.
Yes, this prenatal examination can expose your infant's sex in the very first trimester earlier than any type of ultrasound! The NIPT is carried out with an more easy maternal blood draw, so it poses no threats to you or your infant. As soon as your blood is drawn, it will certainly be sent out to a specific lab whose specialists will examine the results.
Each office could have a various plan for providing results, however someone from your doctor's personnel will likely call you and advice you from there. If you're maintaining your infant's sex a big shock (also to you) until their "birthday," advise your medical providers to keep this information of your NIPT results under wraps.