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.
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PGT-M — Preimplantation Genetic Testing for Monogenic Diseases
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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.
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