Treatments and tests

Prenatal screening for genetic conditions

During your pregnancy, you may be offered a few tests to identify the risk of your baby having a genetic condition.

These include:

  • genetic carrier screening tests for you and your partner
  • screening tests for your baby
  • diagnostic tests for your baby.

It is important to find out if there are any conditions which run in your family that may affect the health of your baby. It is best to do this before you get pregnant but genetic carrier screening is also offered in early pregnancy.

If you are concerned about a particular genetic condition in your family, please talk to your doctor or contact Genetic Services of Western Australia.

Why have prenatal screening?
What is the difference between the tests?
Genetic carrier screening
What chromosomal conditions may be identified?
First trimester screening
Second trimester screening
What do the screening results mean?
Diagnostic tests

Where to get help

  • Your doctor or midwife

To improve the accuracy of the screening program, results and outcomes of pregnancies will be monitored.

Your privacy will be respected, and your personal details will remain confidential.


Acknowledgements

Office of Population Health Genomics

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