What is PGT-M / PGD Testing?
PGT-M, historically called PGD, tests embryos for a specific inherited monogenic disorder so that transfer can prioritise embryos that do not carry the targeted disease genotype when a known familial mutation is present. After IVF and biopsy, embryo samples undergo targeted genotyping; unaffected or appropriate embryos are selected for FET according to counselling and legal frameworks.



