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Preimplantation Genetic Testing (PGT)

Preimplantation Genetic Testing (PGT) is a scientific procedure used to test embryos created through IVF (In Vitro Fertilisation) for specific genetic or chromosomal variations. The embryos are tested before they are transferred to the womb reducing the chance of miscarriages, implantation failures and births with genetic conditions.

Types of PGT

PGT includes three main types of testing: 

PGT-M

(Monogenic/Single Gene Disorders)

This test checks for specific genetic conditions, such as sickle cell anaemia or cystic fibrosis, which may be passed down through families. It is particularly suitable for individuals or families with a known history of genetic disorders. 

PGT-A

(Aneuploidy)

PGT-A is used to detect additional or missing chromosomes in an embryo. It helps reduce the chances of conditions like Down syndrome or Turner syndrome.

PGT-SR

(Structural Rearrangements)

This test identifies issues with the structure of chromosomes, which could lead to repeated miscarriages or difficulties with fertility treatments. 

Types of PGT

You might consider PGT if:

What is the PGT process?

PGT involves the following 8 steps:

This process allows individuals and families to make informed decisions, helping to reduce risks and increase the chances of a successful pregnancy and healthy baby.

At Bridge Clinic, we offer all three types of PGT, and we partner with international reputable genetic institutions to utilise the latest technologies and methods.

How much does PGT cost?

PGT-M

(Monogenic/Single Gene Disorders)

Cost: $11,800*

PGT-A

(Aneuploidy)

Cost: $12,300*

PGT-SR

(Structural Rearrangements)

Cost: $8,950*

*Please note that these costs do not include IVF treatment or prescribed medication.

If you are considering PGT and want to learn more about the process, please contact us or book your consultation today

Preimplantation Genetic Testing (PGT)

Preimplantation Genetic Testing (PGT) is a scientific procedure used to test embryos created through IVF (In Vitro Fertilisation) for specific genetic or chromosomal variations. The embryos are tested before they are transferred to the womb reducing the chance of miscarriages, implantation failures and births with genetic conditions.

Types of PGT

PGT includes three main types of testing: 

PGT-M

(Monogenic/Single Gene Disorders)

This test checks for specific genetic conditions, such as sickle cell anaemia or cystic fibrosis, which may be passed down through families. It is particularly suitable for individuals or families with a known history of genetic disorders. 

PGT-A

(Aneuploidy)

PGT-A is used to detect additional or missing chromosomes in an embryo. It helps reduce the chances of conditions like Down syndrome or Turner syndrome.

PGT-SR

(Structural Rearrangements)

This test identifies issues with the structure of chromosomes, which could lead to repeated miscarriages or difficulties with fertility treatments. 

Types of PGT

You might consider PGT if:

What is the PGT process?

PGT involves the following 8 steps:

This process allows individuals and families to make informed decisions, helping to reduce risks and increase the chances of a successful pregnancy and healthy baby.

At Bridge Clinic, we offer all three types of PGT, and we partner with international reputable genetic institutions to utilise the latest technologies and methods.

How much does PGT cost?

PGT-M

(Monogenic/Single Gene Disorders)

Cost: $11,800*

PGT-A

(Aneuploidy)

Cost: $12,300*

PGT-SR

(Structural Rearrangements)

Cost: $8,950*

*Please note that these costs do not include IVF treatment or prescribed medication.

If you are considering PGT and want to learn more about the process, please contact us or book your consultation today

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