Cellfree Plus Non-Invasive Prenatal Test (NIPT) DNA test lab cost 20000.00 /- Rs

Cellfree Plus Non-Invasive Prenatal Test (NIPT) DNA Test

Cellfree Plus Non-Invasive Prenatal Test (NIPT)

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Reporting Time: 1 Week
Test Cost: 20000.00 /- Rs
Sample Type: 20 ML in Streck tube
Cellfree Plus Non-Invasive Prenatal Test (NIPT) Test Description Cellfree Plus Non-Invasive Prenatal Test (NIPT) Panorama is a Non-Invasive Prenatal Test (NIPT) that screens for Down syndrome and other genetic abnormalities caused by extra or missing genetic information in the baby's DNA*. Panorama is the only non-invasive prenatal screening test that distinguishes between fetal and maternal cell-free DNA thanks to SNP-based sequencing and Natera's proprietary Natus (Next-Generation Aneuploidy Test Using SNPs) algorithm.Only Panorama can distinguish between fetal and maternal DNA in the mother's blood to give you and your patient vital information about the fetus. With a comprehensive panel of chromosomal aneuploidies and microdeletions, Panorama delivers the most accurate results of any screening test, as early as 9 weeks of gestation, to help you manage your patient's pregnancy.

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Cellfree Plus Non-Invasive Prenatal Test (NIPT) TEST DETAILS

Age of the mother is the most common predictor of a higher risk for Down syndrome and several other chromosomal disorders. Medical societies recommend screening for all moms-to-be who are either over 35, have had an abnormal ultrasound, have had a previous pregnancy with a genetic disorder or had a positive maternal serum screen.

Panorama specifically screens for the following conditions and syndromes: Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome) , Trisomy 13 (Patau syndrome), Turner syndrome (Monosomy X) , Sex chromosome trisomies, Triploidy, 22q11.2 deletion (DiGeorge), Angelman, Prader-Willi, Cri-du-chat, 1p36 deletion

The Panorama screening test also looks for certain conditions that carry an equal risk, regardless of the mother's age. Panorama may be appropriate for any mom who is looking for a safe and simple way to learn as much about her baby, without an invasive diagnostic procedure.

You should ask your physician if she/he thinks the Panorama test is a good choice for you.

Vanishing Twin: Only Panorama can distinguish if a vanishing twin's DNA is still present in maternal circulation. The presence of DNA from a vanishing twin cannot be detected using other NIPT methods and can result in an increase in false positive or false negative test results.

Analysis of the maternal contribution: Only Panorama evaluates the maternal genotype in addition to the fetal genotype, thereby providing a clearer result on the pregnancy.

Sex chromosome assessment: Panorama will report sex chromosome trisomies when seen (47 XXX, 47 XXY, 47 XYY).

Triploidy: Only Panorama can detect triploidy as well as provide a risk assessment on every report. This assessment can be beneficial when ultrasound findings are suggestive of triploidy, or for couples seeking recurrence risk assessment following a previous pregnancy with triploidy.

Panorama builds on this technology to provide high sensitivity rates even at low fetal fraction.