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Pharmacogenomics (PGx)
Pharmacogenomic (PGx) testing allows you to personalise your patient’s medication according to their genetic variation.
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Reproductive carrier screening
RANZCOG recommends that information about reproductive carrier screening for common disorders be offered to every woman either prior to conception (preferred) or in early pregnancy.
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Non-invasive prenatal testing (NIPT)
NIPT helps healthcare professionals give expectant parents accurate information about fetal chromosome disorders.
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Lactose intolerance
Sonic Genetics offers a genetic test to assist in the diagnosis of lactose intolerance in both children and adults.
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Familial hypercholesterolaemia
Genetic testing now has a key role in the management of hypercholesterolaemia. Medicare rebated testing is now available through Sonic Genetics.
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Non-invasive prenatal testing (NIPT)
This is a blood test performed on the expectant mother that screens for several common genetic conditions, such as Down syndrome. NIPT is also referred to by some as "NIPS" or non-invasive prenatal screening.
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Lactose intolerance
There is now a genetic test to confirm if you can digest the sugar called lactose found in milk and other dairy products. If you can’t then you are likely lactose intolerant.
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Pharmacogenomics (PGx)
The Sonic PGx panel is a genetic test that helps your doctor to provide the optimal prescription for you based on your genes.
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Reproductive carrier screening
A reproductive carrier screen is a blood test of the parents. It looks to see if they carry genetic changes (mutations) that could cause certain genetic conditions in their child.