dedicated to the treatment of fertility problems
Preimplantation Genetic Testing (PGT)
What is PGT?
Preimplantation Genetic Testing (PGT) is the latest genetic test to identify chromosomal abnormalities or single gene disorder of embryos before implantation to uterus.
Preimplantation Genetic Testing for Aneuploidies (PGT-A) uses array comparative genomic hybridization (aCGH) / next generation sequencing (NGS) to determine if the embryo contains the correct number of chromosomes.
Preimplantation Genetic Testing for monogenic disease/structural rearrangements (PGT-M/SR) is used to test for a specific genetic abnormality when one or both of the couple are carriers of a particular genetic defect.
Day 5/6 blastocyst biopsy
Blastocyst Culture and Transfer
Day 3 embryo biopsy
Blastocyst Culture and Transfer

Indications for PGT-A :
• Advanced maternal age
• Recurrent miscarriage
• Repeated implantation failure
• Previous repeated abnormal pregnancies
• Severe male factor infertility

Indications for PGT-M/SR :
• Couples who are carriers of a monogenic disease or chromosomal disorder (e.g. balanced translocation carrier)

Assisted HatchingFertility Preservation