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Trisomy 21

2019-02-14 14:59:26
On 9th Feb I did my NT Scan where the NT was 2.40 and next day I did the double marker test where the combined trisomy was 1:136. My doctor suggested me another doctor for scan and further consultations where she performed the NT Scan where the NT was 2.30 and combined trisomy is 1:842. 1. How come there is so much of difference in combined trisomy data. 2. Further the doctors suggested to go either for NIPT or Needle test. As I am only 13 weeks pregnant now, not sure which one to opt considering the cons of both. Please suggest.
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Answers (4)

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Answered2019-02-14 15:43:15

YESNO

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You should do amniocentesis as it is more reliable...your reports are showing high value...all the best... connect with me for further query

Answered2019-02-14 15:28:18

YESNO

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NT, Dual marker test, NIPT ARE SCREENING TEST. AMNIOCENTESIS IS DEFINATIVE TEST TO DIAGNOSE CHROMOSOMAL ABNORMALITY IN FOETUS. IN GOOD HAND THERE IS NO PROBLEM TO DO AMNIOCENTESIS.

Answered2019-02-14 17:03:23

YESNO

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Needle  test means  which  one-Chorionic villous biopsy  or Amniocenticis after  some days.  If you want connect for online consultation with me on Practo Consult. 

Answered2019-02-14 17:00:19

YESNO

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