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Dilated Vs Hypertrophic Cardiomyopathy. #cardiomyopathy #drnajeeb #drnajeeblectures #medicaleducation #usmle #mbbslife💊 #medicine Hypertrophic cardiomyopathy (HCM) exhibits left ventricular (LV) hypertrophy with preserved systolic function and impaired relaxation. Dilated cardiomyopathy (DCM) is characterized by increased LV chamber size and systolic dysfunction.
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💔HYpertrophic vs. Dilated Cardiomyopathy: We’ve distilled the essentials into a high-yield comparison table for quick reference. Bookmark this post! ✅ HCM: Asymmetric LV hypertrophy, genetic sarcomere mutations (MYH7, MYBPC3), high SCD risk. ✅ DCM: LV dilation, cytoskeletal defects (TTN, LMNA), poor prognosis if untreated (5-year survival ~50%). 💡- Treatment: Beta-blockers for HCM; ACEI/ARNI SGLT2i for DCM. - Sudden Death Prevention: ICDs critical for HCM; LVEF ≤35% in DCM. 🧬 Genetic Counseli
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💔HYpertrophic vs. Dilated Cardiomyopathy: We’ve distilled the essentials into a high-yield comparison table for quick reference. Bookmark this post! ✅ HCM: Asymmetric LV hypertrophy, genetic sarcomere mutations (MYH7, MYBPC3), high SCD risk. ✅ DCM: LV dilation, cytoskeletal defects (TTN, LMNA), poor prognosis if untreated (5-year survival ~50%). 💡- Treatment: Beta-blockers for HCM; ACEI/ARNI SGLT2i for DCM. - Sudden Death Prevention: ICDs critical for HCM; LVEF ≤35% in DCM. 🧬 Genetic Counseli
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