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Lynch syndrome Module 4 Option 1

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Question 1.

What is your name?

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Question 2.

Once you have identified a patient likely to have Lynch syndrome, you should refer patients for genetic counseling. Where should you refer your patient?

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Question 3.

What are the 3 possible results of genetic testing?

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Question 4.

How can the cancer risk be managed in Lynch syndrome?

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Question 5.

If a pathogenic variant has been found in your patient, can the 1st degree family member (parents, siblings, and children) be offered predictive genetic testing?

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Question 6.

If a Variant of Unknown Significance (VUS) has been found in your patient, can the 1st degree family member (parents, siblings, and children) be offered predictive genetic testing?

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