Преконцепционное генетическое обследование

This is a genetic test using a blood sample. It allows us to examine hundreds of mutations and variants in DNA that cause the most common genetic diseases or have a significant impact on fertility and successful pregnancy.

For whom is the test suitable?

• For couples who are unsuccessfully trying for a baby and want to learn more about their genetic health
• For couples with a family history of a serious genetic condition
• For couples who are unable to conceive or have experienced repeated miscarriages

Testing is suitable for couples using assisted reproduction as well as for those who are trying or want to try for a baby spontaneously. Even though both partners are apparently healthy, they may be carriers of a genetic disease.

Approximate price

€435 per person

What can PANDA Infertility do?

• It can detect the 5 most common rare diseases: cystic fibrosis, spinal muscular atrophy, deafness, fragile X syndrome and phenylketonuria.
• At the same time, it tests genes that give us more information about:
  • the causes of male or female infertility, the degree of ovarian response to hormonal stimulation and the risks associated with the administration of hormone replacement therapy after embryo insertion,
  • the genetic cause of infertility or embryo development disorder,
  • thrombophilic mutation.

How it works

We take blood from both partners and send it to the genetics laboratory, where our geneticists start testing the selected genes. When the 500 most risky genes in the population are examined, 1-2 mutated genes are usually found, which means that a person is a carrier of 1-2 monogenic diseases. The examination ends with a comparison of the mutated genes in both partners, based on which the genetic compatibility of the couple is determined.