Test

What is NIPT Test?
MedGenome Claria NIPT is a simple, safe, and non invasive prenatal screening test that provides assurance to expectant parents with accurate genetic information about their baby. Claria NIPT Test uses advanced bioinformatics technology to evaluate fetal DNA (of placental origin) in maternal blood to identify genetic variations leading to disorders.
What are the conditions that Claria NIPT, NIPT Twins, and Claria NIPT Advanced can detect?
Claria NIPT can detect common Aneuploidies and Sex Chromosome Abnormalities.

Claria NIPT
Trisomy 21 (Down Syndrome)
Trisomy 18 (Edwards’ Syndrome)
Trisomy 13 (Patau syndrome)
Turner Syndrome (Monosomy X/XO)
Klinefelter Syndrome (XXY)
Triple X (XXX)
Jacob’s Syndrome (XYY)
Claria NIPT Advanced
Rare Autosomal Aneuploidies (RAA) include trisomies in chromosomes other than 21, 18 and 13 and monosomies in all 22 chromosomes.
Claria NIPT Advanced screens for RAAs in addition to Trisomy 13, 18, 21 and sex chromosomes.
NIPT Twins
Trisomy 21
Trisomy 18
Trisomy 13