Skip to content
PGT-M — Preimplantation Genetic Testing for Monogenic Diseases
IVF

PGT-M — Preimplantation Genetic Testing for Monogenic Diseases

Specialist physician: Assist. Prof. Dr. Muzaffer Uçarer — Obstetrics & Gynaecology · IVF and Reproductive Medicine  ·  Last updated: June 2026
This page provides general information and does not replace a medical consultation. Please consult your physician about your individual situation.

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.

Prices

  • Per embryo — €400

Our medical prices are fixed; your exact, all-inclusive price is confirmed in writing after your consultation. See our full price list →

Contact UCARER Women’s Health to book your consultation with Assist. Prof. Dr. Muzaffer Uçarer.

Explore More

Related Services

Frequently 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.

Book Now WhatsApp +90 532 262 18 54
Book Now Chat on WhatsApp