PGT-M (Monogenic Disorder Testing)
Screening embryos for specific inherited single-gene disorders.
What is PGT-M (Monogenic Disorder Testing)?
PGT-M screens embryos for specific single-gene (monogenic) disorders known to run in a family, allowing couples at risk of passing on an inherited condition to select unaffected embryos for transfer.
This test is customized for each family based on the specific genetic condition involved.
Is this for you?
How We Treat PGT-M (Monogenic Disorder Testing)
Frequently Asked Questions
Custom test development can take several weeks, so early planning is recommended.
Yes, counselling is an essential part of the PGT-M process to understand implications and options.
Dr. Vedant Jain is an IVF Consultant, Gynecologist, and Certified Embryologist at Asian Navkar Hospital, Indore. Holding post-graduate degrees including an MS and DNB in Obstetrics and Gynecology, he practises reproductive medicine at Asian Navkar Hospital. Dr. Jain specializes in advanced Assisted Reproductive Technologies (ART), complex infertility assessments, low AMH (ovarian reserve) optimization, and fertility preservation. By combining clinical gynecology with laboratory embryology, he works with couples who have had unsuccessful IVF cycles to plan further evaluation and treatment.
Ready for a PGT-M (Monogenic Disorder Testing) consultation?
Share details, our team will call for a private, no-pressure consultation.