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The parents can then choose to transfer embryos that do not have the mutation.

PGD has been in use for over 2 decades, and has been used for several hereditary cancer predisposition syndromes.

However, this is a complex procedure with financial, physical, and emotional factors to consider before starting.

For more information, talk with an assisted reproduction specialist at a fertility clinic.

Now, LFS is thought to be as frequent as 1 in 5,000 to 1 in 20,000.

It allows people who carry a specific known genetic mutation to have children who do not carry the mutation.Regardless of whether a person inherits a mutation or the mutation occurs for the first time in a person, that person has a 50% chance of passing on the normal copy of the TP53 gene and a 50% chance of passing on the mutated copy of the gene to his/her child.A brother, sister, or parent of a person who has a mutation also has a 50% chance of having the same mutation. Options exist for people interested in having a child a prosprective parent carries a gene mutation that increases the risk for this hereditary cancer syndrome.Now, genetic testing is available for people to learn whether they carry a copy of the TP53 mutation before any physical signs of LFS appear. People considering TP53 genetic testing are strongly encouraged to receive professional genetic counseling first, so they can gain the knowledge they need to make an informed decision.This can also help with the serious emotional effects that may occur when people learn that they are a carrier.

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