Combined screening test dating scan

As the risks were so high we got lots of info and were fast-tracked to invasive testing.

There were no major chromosome abnormalities detected, but the wait was the most difficult bit.

And I think for my age, which is, will be thirty five when my baby's born, it's about one in four hundred is the sort of national average. I suppose if it had been good news it would have been nice if they were saying as they were going along, "Well, that looks fine, that looks fine".

And she came back with a piece of paper saying that mine was one in eleven thousand, which felt very reassuring. If it had been bad news I'd probably rather not have known in that position, I'd probably rather be sitting in a room, and sort of take it on board then.

If your result is one in 150 or less, it is considered high.All pregnant women will be routinely offered the nuchal translucency scan as part of their antenatal care.The scan needs to be done between 10 weeks and 13 weeks plus six days gestation, so many hospitals will include the test as part of your 12-week scan. During the scan, the sonographer will measure the amount of fluid at the base of your baby's neck.It is important to remember that after the nuchal scan you are given a percentage of risk, not a diagnosis.It is an indication of the likelihood of Down's syndrome and other genetic abnormalities.

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