Genetic testing in a patient diagnosed with hypertrophic cardiomyopathy (HCM) reveals a mutation in the MYBPC3 gene. This finding suggests a familial form of HCM. What is the recommended advice for the patient's first-degree relatives?

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Genetic counseling and possibly genetic testing.

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Routine echocardiographic screening is not necessary.

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Lifelong anticoagulation to prevent thromboembolic events.

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Immediate initiation of beta-blocker therapy.

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Genetic testing in a patient diagnosed with hypertrophic cardiomyopathy (HCM) re...

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