Nuchal translucency

shell8422

 I didnt do the nuchal screening in my first pregnancy.  I didnt see any real benefit.  I am now 10 weeks pregnant and at the point where I am supposed to have the screening.  Can someone tell me, if something is found to be wrong....is there anything that can be done during the pregnancy to help the outcome?? My Dr seemed to imply that if there was a problem then there are things you can do to help.  Otherwise I dont see the point. 

selahluna

@shell8422 I'm not an OB, but it is my understanding that your NT scan (combined with blood work) can help determine if there are chromosomal disorders by giving you a more specific ratio of chance. Chromosomal disorders are, to the best of my knowledge, not able to be cured. Therefore, I don't think there's anything you can "do to help." These tests, however, can help you prepare either way, by perhaps worrying less, or perhaps allowing you the time to research and be prepared for whatever extra you may need to know or do for yourself and your little love. I hope this helps. 

KLake42

It can prepare you, if you're dealing with chromosomal disorders. For example, babies with Downs sometimes have heart defects, and need immediate surgery after birth. If you have a baby with Downs, you might get additional screening prior to birth to look for heart defects.

crizz13

I learned today at my ultrasound that if there is excess fluid and the chromosomal testing all looks good, the NT measurement can also indicate a heart defect.

BelhurstBride

For my husband and I, we opted to do the testing so, if necessary, we could make arrangements that the proper professionals were present for the birth. 

There isn't anything that can be done to prevent a chromosomal disorder, though some have devastating outcomes if baby even survives to birth. 

soontobemomof6

My daughter had a chromosomal disorder and heart defect. There was an experimental procedure they could do in utero at Boston children's to help correct her defect which would be incurable should she be born with it. You can only do it up to a certain week's gestation, so the earlier you find out, the more time you have to research and decide and get the procedure if you decide. Unfortunately she didn't qualify, but that is one example, though extreme. This is something that should be found at the anatomy scan (but isn't always) and you would still have time to pursue treatment at the point, but I guess the more and earlier screenings you have, the more chance to catch something or at least know to watch out for them.