A set of First Trimester Screenings are done between 10 to 13 +6days weeks of pregnancy to screen the growing fetus for underlying suspect chromosomal abnormalities. This screening requires maternal serum or blood samples for a test that includes a combination of biochemical and biophysical markers.
Combined Screening: This screening combines biochemical (Dual Marker Test) and biophysical (Nuchal transparency & Nasal Bone scan) markers to provide high detection rate of chromosomal abnormalities. The analysed markers are:
Pre-eclampsia Screening: Measures the levels pregnancy-related placental protein A, UAPI, MAF, and PLGF in a pregnant woman’s blood to help predict early-onset of pre-eclampsia
ONTD Screening: biochemical marker: AFP + Ultrasound
Penta Marker Screening: It combines biochemical screening with additional markers for effective diagnosis of chromosomal defects. Its enhanced precision reduces the need for more intrusive methods.
It allows estimating the risk of chromosomal conditions such as Down Syndrome, Edward’s Syndrome,early onset of PE and ONTD
Provides results in just 48 hours
Reduces the need for mother’s to go through high-risk invasive testing
Provides Post-Test Genetic Counselling to understand the results better.
Laboratory Analysis
Testing and analysis of the sample are conducted in the lab.
Reports
The results are shared within 48 hours
Counselling
Post-result free genetic counselling is offered to parents to understand the test results better.
Prenatal Screening - PrePare I
Please note that Prenatal Screening - PrePare I can only be ordered by a physician. They would also be the only person to receive your results and will pass them along to you. If you are unable to find a physician, contact us on 1800-266-5533 & we will organise one for you at no additional cost.