i-screen(Newborn Genome Screen)
Updated: Apr 11, 2022
"Is it all you see on your baby?"
This test screens all chromosomes of the newborn by NGS ( Next Generation Sequencing ) to detect chromosomal abnormalities.
i-screen (Newborn genome screening test) allows your child to be tested early on to find out if he or she is born with a genetic disorder that causes various symptoms such as autism, intellectual disability, and learning disabilities.
(Screen the entire 23 pairs of chromosomes.)
'If I knew in advance ... ' You don't have to regret it anymore.
The more accurately and accurately you can check your baby's genetic diseases, the more you can protect your child.
When a baby is just newborn, you don't feel a big difference from other children,
As the symptoms above may appear gradually,
Get the right treatment roadmap for your child
through the early screening, i-screen !
※Chromosomal disorders are genetic conditions that occur due to a problem with one of the 23 pairs of chromosomes, and there are no cure or treatment in most cases.
That is why it is important to get a faster and more accurate diagnosis for chromosomal disorders to start management therapy.
Test result will be:
1) Not detected - When no disease associated variant was found
2) X Mb deletions/insertions was detected in number N chromosome - When disease associated variant was found.
Download the required documents through the link below!
This test can be performed upon request from a medical doctor.
#i-screen test#i-screen#NGS#Obstetrics#Neonatal Chromosomal Abnormality Screening test#Newborn genome screening