Looking to see if anyone has thoughts on this… at my ultrasound yesterday at 22w6d, the doctor mentioned the nasal bones of the fetuses were “on the small side” and recommended that we do an additional screening for down syndrome. I don’t remember what the screening was called, it’s not an amniocentesis, something else that only requires additional bloodwork. The bad thing is that it’s a new screen that’s not covered by insurance and would cost $200, which is not super expensive, but I would rather not have any unnecessary procedures. The thing is… I’m only 25, and previous screenings came back totally normal with no indications we might have DS. I just don’t think these babies really are at risk for DS, but I wonder if I should spend the $200 and get some peace of mind? It’s kind of bugging me that the fetal doctor found this, but I kinda wonder if she’s being over-cautious and just wants as much testing as possible. I wish I could just forget she ever said anything and look forward to my healthy, normal babies but now I’ll be wondering!
If we decide to do nothing…will we know if they have DS right after they are born?
Re: Doc says fetal nasal bones are small, recommending additional DS screening
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At least they are ID, but is the test accurate with twins? Some of them aren't. However, I'd do the blood test over an amnio any day.
TTC since May 2006. After 3 failed Clomid cycles, 2 failed Injectibles/IUIs, 2 failed IVFs and 1 failed FET, we moved on to adoption!
Last ditch FET resulted in BFP, and identical twin girls!
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would it alter your decision to continue with the pregnancy? If not I would wait it out. Most likely if it is DS there will be more indicators as you progress with the pregnancy. I know a lot of people who refused the test...best of luck.
If your insurance covers ultrasounds, maybe it would make you more confident to have another technician get measurements to confirm that the bones do seem abnormally short, first. Without knowing what measurements your tech obtained, it's tough to say "probably no big deal" or "high probability of DS". While it sounds like there aren't many other risk factors and most of your testing has come back normal, it may be a good idea to have the test (a small percent of DS babies have no other prenatal signs besides nasal bone abnormalities). Length *can* vary by ethnicity, and there is a very small percent of the population with shortened or absent nasal bones who do not have DS, but it may be worth the test just to be able to prepare. If they do have DS, that $200 test is going to be a drop in the bucket. So many people I've met who "wish they would have known" instead of waiting, despite knowing they never would have terminated.
https://www.ncbi.nlm.nih.gov/pubmed/18788563
https://www.jultrasoundmed.org/content/21/12/1387.full.pdf
Right ovary removed 09.04.2012 via vertical laparotomy
Essure implant placed on remaining tube 06.13.2013; successful followup scan 09.30.2013
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