Embryo genetic testing.

Health News

09 May 2022

Embryo genetic testing.
      Embryo genetic testing or Pre-implantation Genetic Testing (PGT) is a test for genetic abnormalities at the chromosome level of the embryo before it is implanted into the uterus. This makes it possible to screen out the abnormal embryos, such as those with the latent gene of anemia, thalassemia, Down syndrome, etc. Currently, using a technology called Next Generation Sequencing : NGS in assays by examining all 23 pairs of chromosomes, the chromosome abnormalities can be known and the sex of the embryo can be known. Therefore, it is suitable for couples with infertility problems and treatment by ICSI has not been successful. The woman is over 35 years old or her family has a history of genetic disease. Some studies have found that embryo genomic testing combined with ICSI also increases the chances of pregnancy.

Embryo genetic testing is useful for the following people:

  • People with genetic diseases or carriers such as thalassemia Down syndrome, etc.
  •  People who have had a child with a genetic disease and want another child without disease.

🛑Please contact for service information and make an appointment before receiving the service.

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