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My wife is 28 years old and is in her 13th week of pregnancy. We had an NT test a couple of days back. The NT was 1.7mm. Trisomy 21 had an adjusted scale of 1:3428. Our doctor has advised us to go for a double marker test. The results will be out in two to three days. Is a risk of 1 in 3428 considered medium to high, to go for a blood test? Is there any relation between double marker test and NT? Is it possible that double marker test results may increase the risk from 1 in 3400s to less than 1 in 300? How are the results of NT and double marker combined? I know it is premature for these thoughts, but the anxiety in waiting for the double marker is killing my wife (and me). I thought of having a first cut understanding of how it works.
The NT (nuchal translucency) test and double marker are dependent on each other.
A risk of 1 in 3428 is not considered high. You have been asked to go for a blood test so as to conclude the results, as only NT test is not sufficient. For the double marker, NT measurement is a must.
With double marker tests, the specific hormones in a pregnant woman's blood are calculated and computed in a graph pattern after taking into consideration the NT measurement, the age of the patient, duration of pregnancy. It is a complex process for you to understand.
I hope that the above answer satisfies you and your wife. Have patience and faith in the God, so that, positive thoughts supervene. Good luck.
Are my NT scan and dual marker test showing any risk in pregnancy? Query:
I am 35 years and in my 13th week of pregnancy. This is my first pregnancy and acheived through ICSI. I had my NT scan and dual marker test was done a week back. The results for the same are NT: 1.10 mm, CRL: 68.2 mm, PAPP-A: 0.18 MOM/0.66 mIU/ml, free beta-hCG: 46.5 ng/ml. I have bee... Read Full »
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Your previous obstetric, gynecology, medical, and drug history matters. Have you been on folic acid daily? If you had any medical issue, was it treated and checked properly? Your nuchal translucency is normal. PAPPA more than 0.5 MOM is normal but you have 0.18. It is les...
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Hi,Welcome to icliniq.com.I have read your question and understand the concerns.The report is showing a high risk for trisomy 21 or Down's syndrome. This first-trimester screening is 95 % sensitive, hence, if the risk is positive, then the amniocentesis should be done to confirm the fetal karyotyp...
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