Nearly 1 in 500 people have hypertrophic cardiomyopathy (HCM), though many remain undiagnosed. Learn the signs and symptoms of HCM. | American Heart Association
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Nearly 1 in 500 people have hypertrophic cardiomyopathy (HC…
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Hypertrophic Cardiomyopathy (HCM) – Diagnosis and Treatment Options
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Start watching the free HCM vodcast series and learn how to better help your patients with hypertrophic cardiomyopathy. | American Heart Association
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Hypertrophic Cardiomyopathy (HCM) is a genetic condition characterized by the thickening of the heart muscle, particularly the interventricular septum. This thickening can obstruct blood flow from the left ventricle to the aorta, a condition known as Left Ventricular Outflow Tract (LVOT) Obstruction. When this obstruction occurs, it is referred to as Hypertrophic Obstructive Cardiomyopathy (HOCM). Key Features of HOCM: Septal Hypertrophy: The thickening of the septum can impede blood flow, leadi
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272K views · 216 reactions | Many with hypertrophic cardiomyopathy (HCM), the most common inherited heart disease, don’t know until their first symptom. | American Heart Association | Facebook
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20 reactions | Apical 4-chamber echocardiogram in a patient with the apical variant of hypertrophic cardiomyopathy (HCM) Apical four-chamber view from a two-dimensional echocardiogram shows apical and midventricular hypertrophy. During systole, the left ventricular cavity is nearly obliterated. | Cardiovascular Education | Facebook
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What is Hypertrophic Cardiomyopathy (HCM)? An inherited condition where the heart muscle thickens, HCM can cause chest pain, palpitations, or even sudden cardiac arrest. On ECG, look for deep Q waves or LVH patterns. 🧬 South Asians – did you know a specific genetic mutation increases your HCM risk 7-fold? 👇 Take our quiz: Which mutation is linked to this? A) APOE ε4 B) MYBPC3 25-bp deletion C) LPA variant D) PCSK9 mutation Drop your answers in the comments! #HCM #Cardiology #HeartHealth #Medic
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