| My wife and I went through this a couple of years ago, with a 10 week NIPT calling a rare trisomy (chr 9), which is always fatal within a few weeks of birth. It was absolute hell. The key problem here is the waiting and uncertainty. You have the NIPT at 10w, but you can’t have the amniocentesis until several weeks later. When that came back fine, there were questions about whether it was a “mosaic” meaning only a small proportion of cells are effected. We were only really in the clear after the 20 week ultrasound. That’s a lot of weeks to be consumed by wondering about whether to terminate the pregnancy, or wait it out for more information. I have a masters in bioinformatics (in genomics!) and my knowledge of stats and the science was next to useless in the face of these decisions. I know of couples who simply couldn’t deal with this uncertainty and chose to terminate on the basis of this test alone. Fortunately for us our child was fine and is a perfectly healthy 18 month old now, but I wouldn’t do the rare trisomy test again. |