In the process of in vitro fertilization (IVF), genetic testing is an important tool for a safer and more successful journey to pregnancy. Thanks to this advanced technology, we can reduce the risk of genetic disorders in the future baby and ensure the best possible embryo selection before proceeding with the transfer.
Why Choose Genetic Testing?
If there is a history of genetic abnormalities in your family or if you simply want to feel more secure during the process, genetic testing can offer you the safety and reliability you need. This testing allows us to identify and transfer only healthy embryos, thus reducing the risk of miscarriage or other complications.
Reducing Risks and Costs
The use of genetic testing not only enhances pregnancy safety but can also reduce the need for multiple IVF cycles, saving time and money. By selecting the healthiest embryos from the start, the chances of success increase, and the need for additional treatments is reduced.
Genetic Tests: Prevention and Diagnosis for Healthy Embryos
Genetic Diagnosis and Analysis
Includes tests such as karyotyping and genetic screening to detect chromosomal abnormalities or genetic diseases. It is used to identify hereditary conditions or abnormalities in parents and embryos.
Fertility and Assisted Reproduction
Tests and treatments related to the assessment and enhancement of fertility to improve the chances of conception through IVF and other reproductive techniques.
Genetic Testing for Diseases
Includes screenings for hereditary diseases, such as cystic fibrosis, and the detection of carriers of genetic diseases that may be passed on to children.
Testing for Genetic Abnormalities and Chromosomal Disorders
Includes tests like Preimplantation Genetic Testing (PGT), which are used for embryo screening and the diagnosis of chromosomal abnormalities or single-gene diseases before implantation.
Are you ready to start your journey?
Whatever your fertility needs, we are here to offer support and guidance every step of the way.
Frequently Asked QuestionsAbout Genetic Testing
What is genetic testing in in vitro fertilization (IVF)?
Genetic testing in IVF involves evaluating the genetic material of the embryo before its implantation in the uterus. The goal is to identify any genetic abnormalities or hereditary diseases that could affect the health of the child.
What are the main methods of genetic testing in IVF?
The most common methods include:
- PGT-A (Testing for Chromosomal Abnormalities): Tests for abnormalities in the number of chromosomes (e.g., Trisomy 21).
- PGT-M (Testing for Monogenic Diseases): Tests for genetic diseases inherited from one or both genes.
- PGT-SR (Testing for Structural Rearrangements of DNA): Examines chromosomal rearrangements that could cause fertility problems or miscarriages.
- Karyotype: Analysis of the entire set of chromosomes to identify chromosomal abnormalities, such as translocations or numerical abnormalities.
- Gene Screen: Tests for common monogenic hereditary diseases, such as cystic fibrosis, sickle cell anemia, and thalassemia, as well as other genetic conditions common in the population.
- Fertiscan: Tests for the identification of genetic factors affecting fertility, such as genetic mutations associated with miscarriages or infertility.
What diseases can be detected through genetic testing?
Genetic testing can detect a range of diseases such as:
- Sickle cell anemia
- Cystic fibrosis
- Thalassemia
- Muscular dystrophy
- Chromosomal abnormalities such as Down syndrome (Trisomy 21)
- Genetic conditions affecting fertility or causing miscarriages (via Fertiscan).
Who are candidates for genetic testing in IVF?
Genetic testing is typically recommended for couples who have:
- A history of hereditary diseases
- Fertility issues or multiple miscarriages
- Pregnancy at an advanced age
What are the benefits of genetic testing?
- Detection and prevention of hereditary diseases
- Increased chances of successful pregnancy
- Reduction in the risk of miscarriage or premature birth
Is genetic testing mandatory in IVF?
Genetic testing is an optional procedure, depending on the individual needs of the couple. However, the treating physician will evaluate the medical history and discuss genetic testing options, recommending the appropriate tests if there are indications or risks for genetic diseases or fertility issues.