Since 2020, aggregated from related topics
Genetic cardiomyopathies are a group of heart disorders that are caused by mutations in genes responsible for the structure and function of the heart muscle. These mutations can lead to abnormalities in the heart muscle, affecting its ability to contract and pump blood effectively. Genetic cardiomyopathies can result in a variety of symptoms, including shortness of breath, fatigue, and an increased risk of sudden cardiac death. Treatment for genetic cardiomyopathies typically involves medication, lifestyle changes, and in some cases, implantation of a pacemaker or defibrillator. Researchers are actively studying the genetics of cardiomyopathies to better understand their underlying causes and develop more effective treatments.