Integrating advanced genetic diagnostics with your fertility journey to lower
risks and maximize your chances of a healthy pregnancy.
Embryos created through IVF are tested before transfer for a known inherited condition or chromosomal change.
A simple blood or saliva test that shows whether you and your partner carry gene changes linked to inherited conditions.
Genetic counselling to help you understand your risks, your testing options and what results mean for you.
Most people who carry a genetic change are healthy and unaware of it. Screening before or during fertility treatment can help you understand whether there is a chance of passing on certain conditions, and what choices are available.
Our genetic counsellors and specialists explain every step, so the information you receive is useful, not overwhelming.
Anyone planning a pregnancy can consider carrier screening. It is particularly relevant if there is a known condition in the family or if partners are related.
Screening shows whether there is an increased chance of a condition. Diagnostic tests confirm whether a specific condition is present.
Carrier screening results usually take a few weeks. If PGT is used, embryos are frozen while results are processed and transferred in a later cycle.
Yes. We recommend counselling before and after any genetic test so that you can make informed decisions.
You don't have to have every answer before you
reach out. We're here to help you understand your options.
