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Preimplantation Genetic Testing

Embryo Genetic Testing (PGT)

Chromosomes or genes of embryos are tested before transfer to help physicians select embryos suitable for transfer. It covers three categories: aneuploidy screening, monogenic disease testing and chromosomal structural rearrangement testing.

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Laboratory Technology

Embryo Genetic Testing (PGT)

Chromosomes or genes of embryos are tested before transfer to help physicians select embryos suitable for transfer. It covers three categories: aneuploidy screening, monogenic disease testing and chromosomal structural rearrangement testing.

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Embryo Genetic Testing (PGT)
Who Is It For

When This Service Is Considered

The following is for reference only; suitability must be determined by a physician based on test results.

Female age 38 or above, with increased risk of embryonic chromosomal abnormality

Two or more miscarriages or repeated implantation failure

One partner carries a balanced translocation, Robertsonian translocation or inversion

A clear family history of monogenic disease or carrier status

A previous pregnancy with a chromosomally abnormal fetus

Process Schedule

The overall process is as follows; actual milestones are adjusted according to test results and individual response.

01

Genetic Counseling

Review family and pregnancy history to determine the type of testing

02

Plan Confirmation

Determine PGT-A / PGT-M / PGT-SR and the applicable technical pathway

03

Blastocyst Biopsy

A small number of trophectoderm cells are taken at the blastocyst stage, with freezing completed at the same time

04

Laboratory Testing

Samples are sent to a specialized genetics laboratory for amplification and sequencing

05

Report Interpretation

A genetic counselor and physician interpret the report together, explaining usable embryos and limitations

06

Transfer Decision

Frozen-thawed embryo transfer is scheduled based on the report and endometrial condition

Technical Highlights

These are our specific requirements at the execution level, and they can also be inspected on site during a visit.

Three Testing Categories Covered

Supports aneuploidy screening, monogenic disease and chromosomal structural rearrangement testing

Standardized Biopsy Timing

Trophectoderm biopsy at the blastocyst stage, performed by senior embryologists

Transparent Reporting

Clearly states the testing scope, methodological limitations and mosaicism findings

Genetic Counseling

Genetic counseling is provided before and after testing to help you understand the results

Common Questions About This Service

No. PGT tests chromosome number, specific structural abnormalities or known pathogenic variants; it cannot cover all genetic diseases and does not replace routine prenatal screening and diagnosis during pregnancy.

A genetic counselor should explain the risks and priority based on the specific situation; it is usually not the first choice.

Embryos are frozen after biopsy; the report usually takes several weeks, after which a separate transfer cycle is arranged.

The content of this site does not constitute medical advice. Assisted reproduction offers no guaranteed outcome; the specific plan is subject to in-person assessment by a licensed physician.

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Want to Know Which Plan Fits You?

Send your test reports and we will provide a preliminary assessment and timing recommendations.

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