What is NIPT, and is it a diagnostic test or a screening test? Get the answers to these questions in this video as Dr. Nagarathna - MBBS, DGO, Obstetrics & Gynecology - talks about NIPT.
Respected doctor i lost my baby she is carried immunodeficiency,,,, now my wife is 6 week pregnant ,, so doctor what is the best test NIPT or amniocentesis in this case
Seems like these tests are useless if they are just for screening purpose. If the chromosomal abberations can be seen under the microscope why do we keep parents in dilemma and ruin their entire pregnancy journey
This is not a useless test, to check the chromosomes of the fetus invasive procedure like amniocentesis/ chorionic villus sampling is required which itself has some risk of miscarriages, it is not ethical to recommend every pregnant women to go though invasive procedure to know the common chromosomal problems. These screening test help in determining who needs further confirmatory test and who doesn’t.
Hi mam. good morning.. 1 live 4yrs baby iruku sir.. 3 spontaneous abortion sir G5 ipo.. NT 1.2mm normal, nasal seen Double marker test la Trisomy 21 cut off1:250, mom 1.98 Trisomy 18/13 cut off 1:100, mom 0.5 Iruku high risk positive vandu iruku mam Nan LMWH 0.4ml od eduthutu iruka mam. Na NIPT test panalama? Illa aminocensis d panradu best a mam? Pls rply me mam
Respected Doctor, in 7 months scanning report of my daughter-in-law, AFI Level increased to 25 and 38 weeks 2 days Scanning Report again increased to 31.5. What to do Doctor. She is in her mother's house at Kumble, Kasaragod.
Mem my age 34. Dable marker test lo biochemical T21 1:207 undi doctor nipt chepinchukommannaru yemina problem avuthudaaaa?? Please 🙏 cheppandi please please
Hi, I have undergone double marker test, which has given results at low risk, when consulted my Gynaecologist, she said we can NIPT but on the other hands , she says everything is normal. Please suggest what to do.
I have given sample of nipt the sample got lysed what's the reason can u explain ... And the sample drawn was very forceful manner is that the chance of sample getting lysed ... ?
Ma'm I m 18 week pregnant and my ultra sound report is "single live fetus of 18 weeks 01 day +/- 2 weeks maturity with right choroid plexus cyst, bilateral mild pyelectasis and echogenic focus in lv." Ma'm pls tell me this report is good or bad.
My wife age is 23years. Taken NT scan at 13 weeks 2days. NT 2.5mm. Mild increased in thickness. Done the double marker test also and double marker test is negative. Is there any problem to baby?? Is NIPT test compulsory. Kindly reply me.
My NIPT result got with trisomy 21 risk...now waiting to do amniocentesis. Anybody is here with amniocentesis report came no risk thought NIPT report is high risk?
@@Publicchannel5 Get advice from your doctor. Here is my personal view and I am not a doctor - Its accuracy is around 99%. If its positive then you should go with amniocentesis. False negatives are there in nipt but that's very rare. You can go through this best info video on nipt - ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-tJg8mJeKLwY.html
Dr . We have been told our NIPT test has come out with High risk- Trisomy 21 detected. Now we have give out sample for amniocentesis . Waiting for the results. What are out chances of having a normal healthy baby. ?
