This is a non-invasive assay used for the detection of Fetal trisomies like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18) and Patau’s syndrome (Trisomy 13) using Maternal peripheral blood. In addition the assay detects 20 different types of Microdeletion syndromes like DiGeorge, William, Prader Willi, Angelman etc. The specificity of the test is >99% with a false positive rate of <0.05%.

10 mL Whole blood in a special tube available from TrueMedix. Ship refrigerated. DO NOT FREEZE. Valid between 10-24 weeks of gestation. Duly filled Form G AND MBFD/NIPT consent form (Form 21) is mandatory. Samples shall be accepted only from registered genetics clinics under PCPNDT Act.

DNA Sequencing

8 To 10 Days

*Trisomy detection for 13, 18 & 21 Chromosomes *20 Microdeletion syndromes

Test is valid between 10-24 weeks of gestation. Duly filled MBFD/NIPT consent form (Form 21) is mandatory.