NIPT- (All Chromosomes and Microdeletions)

Jananya Non Invasive Prenatal Screening Test (NIPT) All Chromosomes and five microdeletion syndromes

It analyses the cell free fetal DNA present in the maternal blood for the presence of chromosomal aneuploidies

The expectant mother’s blood is drawn and sent to the laboratory for testing. It is important to send the latest sonography reports, clinical history

The test can be done anytime after 10 week pregnancy.

The expectant mother’s blood is drawn and sent to the laboratory for testing.

No Risk

The report will indicate the probability of a baby being born with the screened chromosomal conditions. Results are provided as scores that is compared to normal and below normal ranges. The probability of risk is given as: – Low risk: The pregnancy is unlikely to be affected by aneuploidies that were screened. – High risk: The pregnancy is likely to be affected by trisomy or aneuploidy. Further confirmatory tests will be required. – No result: May occcur due to insufficient (less than 3.5% fetal fraction) placental DNA in the sample. In the event of a positive test result, your healthcare provider will discuss further diagnostic options for a definitive diagnosis such as: – High-resolution ultrasound – Chorionic villus sampling (CVS) – Amniocentesis