Embryo chromosome test increases the chance of pregnancy and reduces miscarriage. In older mothers

Embryo chromosome test increases the chance of pregnancy and reduces miscarriage. In older mothers

Chromosomal abnormalities in embryos are considered the main cause of miscarriage in the first trimester of pregnancy (miscarriage), which occurs in 60% of all spontaneous abortions. Currently, the technology for treating infertility has advanced to the point where it is possible to diagnose genetic diseases in embryos before they are reinserted into the uterus. It can increase the chances of a complete pregnancy and reduce the rate of miscarriage due to the baby’s genetic disorders.

The analysis detects abnormalities at the chromosomal level by screening the chromosomes of 23 pairs of embryos to select the healthiest embryo and reinsert it into the uterine cavity. With Next Generation Sequencing or NGS technique, it is the latest technology with high accuracy. It also reduces the risk of miscarriage. Reduce the chance of developing severe genetic diseases such as Down syndrome, etc.

Who can benefit from a chromosomal screening?

1. Female patients over the age of 35 years due to a high risk of giving birth to a child with chromosomal abnormalities.
2. Spouses who have had a history of childbirth and find that their children have chromosomal abnormalities.
3. Couples with a history of more than 2 miscarriages before 12 weeks of pregnancy
4. Male/female patients with a family history of genetic disorders
5. Couples who have treated infertility with IVF but have not succeeded more than 2 times.

If you are interested in the package of the Medical Center for Childbirth, click

Thank you for the content from:

Dr. Veena Krudsawat