Why PGD is so important?
PGD improves pregnancy rates by identifying the presence of certain kinds of genetic disorders which can seriously affect the health of a baby. PGD/PGS testing are recommended for couples that have a family history of inherited disease or recurrent IVF failures, recurrent pregnancy loss, advanced maternal age or any genetic conditions.
When is PGD Recommended?
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A family history of hereditary genetic disorders.
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Previous cases of children born with genetic conditions.
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Maternal age over 35 years.
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Failed IVF cycles due to genetic causes.
Advantages of PGD:
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Detection of mutations in specific genes causing genetic disorders (e.g., cystic fibrosis, hemophilia, thalassemia, etc.).
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Reduced risk of passing on hereditary diseases.
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The ability to select a healthy embryo for implantation.
PGD, PGS
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PGD 5
A PGD5 is recommended to check most frequent chromosomal abnormalities in embryos. PGD5 allows testing of embryos for certain characteristics:
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(X, Y) Gender selection
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(13) Patau Syndrome
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(18) Edwards Syndrome
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(21) Down´s Syndrome
PGD 9
PGD9 tests 9 pairs of chromosomes (X, Y, 13, 15, 16, 17, 18, 21, 22). This involves studying a certain number of chromosomes, which are the locations of the most commonly found aneuploidies.
PGD 24
PGD 24 allows to prevent the birth of a child with chromosome diseases and decreases the risk of miscarriage. In order to carry out the preimplantation genetic diagnosis, the FISH analysis (fluorescent in situ hybridization), PCR analysis (polymerase chain reaction) or CGH analysis (comparative genomic hybridizations) are usually used. The geneticist doctor chooses the method for the PGD procedure in each specific case.
Ready to Start Your Journey?
We are here to help you achieve your dream of parenthood. Our team is ready to work with you, using the latest technologies and expert knowledge, to make your dream come true.
Contacts
+38 (093) 008 02 21
Dmytra Chyzhevskoho St, 2V,
Kyiv, Ukraine