Safe and Accurate Solution For Every Pregnant Women and Baby
(Non Invasive Prenatal Test)
To test for chromosomal abnormalities in the fetus, G-NIPT analyzes cell-free fetal DNA in the blood of a mother by NGS (Next Generation Sequencing).
G-NIPT screens for all chromosomes including Down Syndrome, Edward Syndrome, Patau Syndrome, Sex Chromosome Anueploidies, and Microdeletions.
Fragile-X Screening Test
Essential screening Test for those who plan for a healthy baby. Analyzing whether parents have the same Fragile X syndrome carriers or not. Fragile X syndrome is one of the most common hereditary disease that causes mental retardation. Even if the mother does not have Fragile X symptoms, the child can be affected.Affects about 1 in 4,000 males / Affects about 1 in 8,000 females
Type 1 Myotonic Dystrophy Test
Essential screening Test for those who plan for a healthy baby. Analyzing whether parents have the same Myotonic Dystrophy carriers or not. Myotonic Dystrophy is one of the most commonly found hereditary neuromuscular diseases. The affected fetus has a higher risk of premature birth and respiratory difficulties. Affects about 1 in 8,000.