NMCK wants to you have a healthy baby

Every year, many parents are born because they do not know that they have a genetic disease gene, and babies with a genetic disease are born. To this end, NMCK cooperates with the world's most authoritative genetic testing research center to provide an advanced specific gene carrier detection, Couples' genes can be tested before pregnancy to inform them in advance of the risk of having a baby with a serious genetic illness

What is CGT Test?

1. CGT (Test for Specific Gene Carriers) is an important test before planning pregnancy.
2. It can examine whether a couple is likely to pass on hereditary diseases to their children. A simple DNA test before pregnancy can avoid passing on hereditary diseases to the next generation.
3. Advanced tests will tell us if parents carry one or more recessive genetic mutations to confirm that you will have a happy and healthy pregnancy.
4. The CGT test finds diseases such as cystic fibrosis, spinal muscular atrophy, fragile X syndrome, etc. through NGS analysis.

Why do CGT Test?

1. Parents usually realize they are the cause of a serious genetic disorder only after the child is born.
2. Because carriers are usually healthy, children can be affected when both parents carry mutations in the same gene.
3. Most genetic diseases cannot be cured, but they can be prevented by CGT testing.

Who is suitable for CGT testing?

1. If you have a family history, you want to know before your pregnancy that your baby may be at risk for a family inherited disease.
2. If you are about to start an assisted reproductive program.
3. If you are preparing to receive a sperm or egg donation, we recommend that you consider performing a CGT test.