Lynch syndrome Module 4 Option 1

Refer your patient to your in-house mainstreaming service if you have one set up
Refer your patient to your linked specialized clinical genetics centre
I can refer to either of the above
None of the above

The patient have Lynch syndrome, the patient doesn't have Lynch syndrome, or we are unsure whether the patient has Lynch syndrome
A pathogenic variant being identified, a pathogenic variant not being identified, and a variant of unknown significance being identified
This is incorrect, there are 4 possible results
Positive or negative

2 yearly colonoscopy
A daily low dose of aspirin, one-off testing for H. pylori, and lifestyle recommendations
Risk-reducing surgery
All of the above

Yes, but 2nd degree relatives can also be offered predictive genetic testing
Yes, to find out if the relatives have Lynch syndrome too
No, even though we are certain that the patient has Lynch Syndrome
No, because we are not sure if the variant is benign or likely to be responsible for their cancer