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Search results for: "Genetic Testing"

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Genetic counselling

Genetic counselling can be helpful for some people when planning or during pregnancy. Find out about genetic counselling and what to expect.

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Genetic carrier screening

Screening for carrier status is a blood test to see if you carry genes that are linked to certain health conditions. Learn more about this test here.

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What is a congenital disorder?

Congenital disorder, also known as congenital disease or birth defects, are conditions present from birth. Find out more about congenital disorders.

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Non-invasive prenatal testing (NIPT)

A non-invasive prenatal test (NIPT) is a sensitive test to screen for Down syndrome and some other chromosomal disorders early in pregnancy.

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Screening for Down syndrome

Down syndrome is a common chromosomal disorder. Find out about the screening and diagnostic tests to detect the condition before your baby is born.

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Amniocentesis

Amniocentesis is a diagnostic test, done during pregnancy, to assess whether the baby has an abnormality or serious health condition. Find out what’s involved.

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Prenatal screening (genetic screening in pregnancy)

Prenatal screening tests assess the chance of some medical problems your baby may have. Your healthcare provider can help decide if they're a good idea.

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Cystic fibrosis (CF)

Cystic fibrosis (CF) is a genetic disease that affects your lungs and digestive system. Learn more about what causes CF and how it is treated.

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Fragile X syndrome

People with Fragile X syndrome have intellectual disability, behavioural and learning challenges as well as certain physical characteristics.

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Prenatal screening and testing

Prenatal testing is available to check the health of your baby. It is your choice if you decide to have these tests and you should discuss your options with your doctor or genetic counsellor.

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