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PGTA/PGTM, PGT-SR

PGTA/PGTM, PGT-SR

PGT-A, PGT-M, and PGT-SR are preimplantation genetic tests performed before embryo transfer to evaluate genetic health.

These tests provide important information about embryos and help improve IVF success rates.

PGT-A

PGT-A detects chromosomal abnormalities (aneuploidy).

A healthy embryo contains 46 chromosomes (23 pairs). Any abnormal number increases the risk of implantation failure or early miscarriage.

PGT-M

PGT-M identifies inherited genetic diseases caused by mutations in a single gene.

It is used when:

  • Both partners are carriers of a genetic condition
  • One partner has a hereditary disease
  • There is a family history of genetic disorders
  • A previous child has a genetic disease

PGT-SR

PGT-SR detects structural chromosomal abnormalities such as:

  • Translocations
  • Inversions

These abnormalities may negatively affect embryo development and pregnancy outcomes.

Frequently asked question

Schedule a consultation with our fertility experts and take the first step toward your parenthood journey.

Schedule a consultation with our fertility experts and take the first step toward your parenthood journey.

Schedule a consultation with our fertility experts and take the first step toward your parenthood journey.

Schedule a consultation with our fertility experts and take the first step toward your parenthood journey.

Schedule a consultation with our fertility experts and take the first step toward your parenthood journey.