HealthCareMagic is now Ask A Doctor - 24x7 | https://www.askadoctor24x7.com

Get your health question answered instantly from our pool of 18000+ doctors from over 80 specialties
159 Doctors Online

By proceeding, I accept the Terms and Conditions

Dr. Andrew Rynne
MD
Dr. Andrew Rynne

Family Physician

Exp 50 years

HCM Blog Instant Access to Doctors
HCM BlogQuestions Answered
HCM Blog Satisfaction

What Could Trisomy 21 Test Findings During Pregnancy Be Suggestive Of?

I am 20 weeks pregnant now, the trisomy 21 test showed 1:235, which said there is an increased risk, but my doctor is confident says she's confident on the Ultra scan of gravid uterus test which says N T=2mm;. But still she suggested me to go for 2nd opinion. what do you say? I am 29 yrs old. 5.3' & 68 kgs
Tue, 28 Apr 2015
Report Abuse
OBGYN, Maternal and Fetal Medicine 's  Response
Hi, I have gone through your question and understand your concerns. A risk of 1:235 of trisomy 21 is not a very high risk, however it is more than normal which is 1:250. Moreover, NT of 2 mm is just borderline for increased risk of trisomy 21.
I would suggest you to consult a fetal medicine specialist and get a detailed anomaly ultrasound. If any soft markers of trisomy 21 is present in the fetus, then you should undergo amniocentesis to confirm the fetal karyotype. Further management has to be done accordingly.
Hope you found the answer helpful.
Wishing you good health.
Dr Deepti verma
I find this answer helpful
Disclaimer: These answers are for your information only and not intended to replace your relationship with your treating physician.
This is a short, free answer. For a more detailed, immediate answer, try our premium service [Sample answer]
Share on
 

Related questions you may be interested in


Recent questions on Aneuploidy


Loading Online Doctors....
What Could Trisomy 21 Test Findings During Pregnancy Be Suggestive Of?

Hi, I have gone through your question and understand your concerns. A risk of 1:235 of trisomy 21 is not a very high risk, however it is more than normal which is 1:250. Moreover, NT of 2 mm is just borderline for increased risk of trisomy 21. I would suggest you to consult a fetal medicine specialist and get a detailed anomaly ultrasound. If any soft markers of trisomy 21 is present in the fetus, then you should undergo amniocentesis to confirm the fetal karyotype. Further management has to be done accordingly. Hope you found the answer helpful. Wishing you good health. Dr Deepti verma