Considerations To Know About NIPT Scan
Cell-free DNA (cfDNA) arises from the natural breakdown of fetal cells (presumed to be primarily placental). The NIPT analyses cell-free DNA in the maternal blood which can show the probability of Down's syndrome (Trisomy 21), Edwards Syndrome (Trisomy 18) and Patau's Syndrome (Trisomy 13). On demand we can likewise yield a result for the gender of your infant, all from a maternal blood sample.
Really periodically it might involve transvaginal/ internal scanning. Includes: thirty minutes visit A scan for viability (heart beat) and gestation measurements A maternal blood sample (from the arm) taken into 2 sample bottles Ultrasound Direct toMOBILE shipment of your scan images and report Digital ultrasound report 2D ultrasound b/w prints in sleeve on the day, fetal DNA blood results roughly 7 working days later on Plus complimentary sexing if requested either with ultrasound * (from 16 weeks pregnancy or later on) on the day website or consisted of with your blood test outcome (from 10 weeks) Plus 4DFREEVIEW (from 12 weeks) with 3D ultrasound b/w prints click here in sleeve ** If you want to know the sex of your baby we will give you our expert viewpoint with this scan If your infant's position is not beneficial to do this on the day however, we can not use a complimentary rescan for this purpose.
Please note that 4DFREEVIEW is a complimentary option and if your baby's position is not click here favorable for aesthetics on the day, we can not use a free rescan for this factor. Need to expose lower abdominal area so ideally use different garments i. e pants or skirt and top. Consume 0. 5 Ltr (1 pint) clear fluid approx 1 hour before consultation time.
The NIPT is analysed in the UK by our authorised partners: Consistency by means of TDL. In scheduling a NIPT consultation with us you are concurring to your personal information being shown the appropriate partners solely for the function of this test. Your express permission will also be asked for throughout your appointment.