genetic cardiomyopathy

Genetic cardiomyopathy is a heart condition caused by inherited gene mutations that affect the heart muscle’s structure or function. These changes can lead to thickened, weakened, or stiffened heart muscles, impairing the heart’s ability to pump blood effectively. It often runs in families and may cause symptoms like fatigue, shortness of breath, or fainting. Because it’s inherited, family members might also be at risk. Diagnosis involves genetic testing and imaging studies, and management includes regular monitoring, lifestyle adjustments, medications, and sometimes devices or surgery to prevent serious complications.