PGT-A reflex to PGT-M (variant 2)- 10 Embryos

PGT-A Reflex to PGT-M (Variant 2) – 10 Embryos

PGT-A Reflex to PGT-M (Variant 2) – 10 Embryos is an advanced preimplantation genetic testing service that first screens up to 10 embryos for chromosomal abnormalities (PGT-A). If required, testing automatically extends to PGT-M (Variant 2) to detect a specific inherited genetic variant identified in the family. This combined approach helps improve embryo selection and supports informed reproductive decisions during IVF treatment.

Why is this test done?

• Screens embryos for chromosomal abnormalities.
• Detects a known inherited genetic variant (Variant 2).
• Helps reduce the risk of passing on genetic disorders.
• Improves selection of genetically suitable embryos for transfer.
• Supports personalized IVF treatment planning.

Sample Required: Embryo biopsy sample (collected by the IVF clinic)
Method: Next-Generation Sequencing (NGS) with reflex PGT-M analysis
Recommended For: Couples undergoing IVF with a known familial genetic variant and requiring both chromosomal and targeted genetic screening.