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We tell you all about pre-implantation genetic testing
PGT - WHAT IS THAT?
Preimplantation genetic testing (PGT) is a method for identifying embryos with gene and/or chromosome abnormalities.
PGT HAS A POSSIBLE
Prevent the birth of a child with chromosomal diseases.
Reduce reproductive losses during pregnancy.
Increase the effectiveness of IVF.
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RECOMMENDED
Mother's age >35 years.
Habitual pregnancy failure.
Multiple failed IVF attempts.
Some forms of male infertility associated with chromosomal abnormalities.
Carrying chromosomal rearrangements, translocations, inversions, and other chromosomal abnormalities.
FREQUENCY OF CHROMOSOMAL ABNORMALITIES IN FEMALE EMBRYOS
According to statistics, after one IVF protocol, children are born in 41% of cases.
The percentage increases to 69% when PGT is performed.
The couple goes to the clinic and undergoes IVF preparation and egg and sperm biopsies
The egg is fertilized with a sperm cell
on day 5 of embryonic development, a biopsy is taken and 3-5 cells are taken for examination
The sample is sent to the TreeGene laboratory in Almaty
the embryo is frozen by cryopreservation
NGS genetic study is performed within 2-4 days
the finished result is sent to your doctor
If the embryo passes the selection criteria, it is transferred into the uterine cavity
the process ends with a long-awaited pregnancy
High resolution by nucleic acid sequencing.
Potential for simultaneous diagnosis of chromosomal and monogenic pathology.
A more sensitive method than aCGH, it can detect 20% mosaicism, numerical and structural abnormalities of chromosomes.
Quantitative analysis of mitochondrial DNA.
Fast technology with results the next day.
CONTACT
1 embryo - 141 500 tenge