Preimplantation Genetic Testing

Preimplantation Genetic Testing (PGT) evaluates embryos before transfer to identify genetic conditions and support informed IVF decisions.
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Understanding Preimplantation Genetic Testing (PGT)

Preimplantation Genetic Testing (PGT) refers to a set of genetic tests that are performed on embryos prior to their transfer to the uterus. At Anderson Diagnostics, we offer various types of PGT, each designed to detect specific genetic conditions or traits:
PGT-A will now be used to describe screening embryos for sporadic chromosome abnormalities, instead of PGS and CCS.
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PGT-SR will now be used to describe chromosomal PGD. This is different from PGT-A, as in these cases the chromosome abnormalities.
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PGT-M is used to help individuals or couples reduce their risk to have a child with a known inherited disorder caused by mutation.
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Non-invasive preimplantation genetic screening (NiPGS) is used during in vitro fertilisation (IVF) to evaluate embryos for chromosomal abnormalities.
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