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Even if you are perfectly healthy, if you have an inherited disease in your family history, you need to know your options…

Fertility > We want to prevent inherited diseases

We want to prevent inherited diseases

Are you a health specialist?
What Is your family history? If you or a close family member have a single gene disease you may wish to reduce the risk that your child inherits that disease.
Even if you are perfectly healthy, it is possible that genetic testing could determine that you are a carrier, at an increased risk to have a child with a genetic disease.
Preimplantation Genetic Testing for Monogenic Disease (PGT-M, formerly called PGD) can be used to test embryos for a specific single gene disease such as cystic fibrosis, Tay-Sachs disease, spinal muscular atrophy (SMA) and sickle cell. PGT-M can test embryos for almost any known single gene disease and help your doctor determine which embryo is most likely to be unaffected by that specific disease.

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Prevent Inherited Diseases

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What is the difference between a syndrome and a disorder?
20 September, 2020
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Path to Fertility

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CGT

Carrier Genetic Test
Determines the risk of having a child with a
genetic disease

More information

PGT-M

Prevents the transmission of single gene disorders

More information

Sex selection and Sex determination, before and after conception is prohibited and punishable under PC & PNDT act no. 57 of 1994

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