PGT-M is used when one or both partners carry a known genetic condition that could be passed to the child — for example thalassaemia, cystic fibrosis, or familial cancer-related mutations. The embryo is tested for that specific gene before transfer, allowing only unaffected embryos to be selected. Each PGT-M case is preceded by a genetic counselling step and a custom-built laboratory protocol.
IVF
PGT-M — Preimplantation Genetic Testing for Monogenic Diseases
Explore More
Related Services
How Successful Is the Drug-Free IVM Method?
IVM (In Vitro Maturation) is a fertility treatment alternative where immature eggs are collected with minimal or no hormone stimulation, then matured in a laboratory.
Learn MoreEndomeTRIO — Triple Endometrial Analysis
EndomeTRIO combines ERA, EMMA and ALICE tests in a single biopsy to reveal why an embryo may not implant.
Learn MoreMicro TESE
Male infertility affects approximately half of infertile couples. Micro TESE is an advanced sperm retrieval procedure performed under microscopic visualization.
Learn MoreFrequently Asked Questions
Common Questions
Couples where a single-gene inherited condition is known in the family or confirmed by carrier testing.
Yes. Counselling is essential before designing a PGT-M test for your specific case.
Several weeks to months, depending on how rare the gene is.
Yes, after your written consent and discussion of all results.
Yes, often it is, for the most informed selection.
Book Your Appointment Today
We provide a comfortable environment where you can consult us with all your problems in the field of Obstetrics, Gynecology and IVF Treatment.