thayet
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Just wondering if anyone has had any experience with this..
On the 12 week ultrasound, the baby's NT measurement was 3.1mm. I panicked and opted for the non-invasive Harmony test (also called MaterniT21 in the US) and the results came back clear (ie. no probable trisomies detected). Now I just got the results back from my integrated prenatal screen and was given a 1:8 risk of Down's.
Has anyone had as high a risk as 1:8 and had a healthy baby? There were no other soft markers for genetic abnormalities on the ultrasound, as far as I know. I have an appointment with a genetics counselor tomorrow. Thanks.
On the 12 week ultrasound, the baby's NT measurement was 3.1mm. I panicked and opted for the non-invasive Harmony test (also called MaterniT21 in the US) and the results came back clear (ie. no probable trisomies detected). Now I just got the results back from my integrated prenatal screen and was given a 1:8 risk of Down's.
Has anyone had as high a risk as 1:8 and had a healthy baby? There were no other soft markers for genetic abnormalities on the ultrasound, as far as I know. I have an appointment with a genetics counselor tomorrow. Thanks.