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General Medicine · Cardiology: hypertrophic cardiomyopathy
Sample itemWhich statement about hypertrophic cardiomyopathy is correct?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. It is autosomal dominant from sarcomere gene mutations and is the commonest cause of sudden death in young athletes
HCM is inherited as autosomal dominant, most often through beta-myosin heavy chain or myosin-binding protein C mutations. It is a leading cause of sudden cardiac death in young athletes. Vasodilators, diuretics in excess and digoxin worsen outflow obstruction.
Option by option
A. It is autosomal dominant from sarcomere gene mutations and is the commonest cause of sudden death in young athletes (correct)
Correct. This summarises inheritance and sudden death risk.
B. It is treated with vasodilators and digoxin
Vasodilators and inotropes increase the gradient.
C. It is X-linked recessive
Inheritance is autosomal dominant, not X-linked.
D. It shows thin dilated ventricular walls
Wall thickening, not thinning, is characteristic.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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