Cardiomyopathy is a disease of the heart muscle (myocardium) that makes it harder for the heart to pump blood to the rest of the body. It can lead to heart failure or irregular heartbeats (arrhythmias).
Dilated Cardiomyopathy:
The heart chambers enlarge and weaken, reducing the heart’s ability to pump blood efficiently.
Hypertrophic Cardiomyopathy:
The heart muscle thickens abnormally, making it harder for the heart to work properly.
Restrictive Cardiomyopathy:
The heart muscle becomes rigid and less elastic, limiting the heart’s ability to fill with blood between beats.
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC):
Rare condition where heart muscle is replaced by fatty or fibrous tissue, affecting electrical signals and causing arrhythmias.
Genetic mutations (inherited conditions)
Long-term high blood pressure
Heart tissue damage from heart attacks
Infections or inflammation of the heart
Alcohol abuse or drug toxicity
Metabolic diseases such as diabetes or thyroid disorders
Shortness of breath
Fatigue and weakness
Swelling in legs, ankles, and feet
Irregular heartbeat or palpitations
Chest pain or pressure
Dizziness or fainting
Physical examination
Electrocardiogram (ECG)
Echocardiogram (ultrasound of the heart)
MRI of the heart
Blood tests
Genetic testing in some cases
Lifestyle changes (diet, exercise)
Medications to improve heart function and control symptoms
Devices like pacemakers or defibrillators
Surgery or heart transplant in severe cases
The term "cardiomyopathy" comes from Greek roots: kardia (heart), myo (muscle), and pathos (disease).
Recognition of cardiomyopathies as distinct heart diseases evolved throughout the 20th century as medical imaging and pathology improved.
The first detailed descriptions appeared in the 1950s-1960s, with advances in understanding genetic causes emerging later.
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