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- W4205245068 abstract "This chapter discusses the heart diseases that are deemed to be due to inherited changes. Hypertrophic cardiomyopathy (HCM) is usually a familial disease of genetic origin, characterized by alterations in proteins of the myocardial cells leading to myocardial fiber disarray, hypertrophy of the heart, and an increased incidence of sudden death. In contrast to what is observed in the inherited long QT syndrome, in HCM, it is not possible to predict the different mutations based on the electrocardiogram changes, and vice versa, except for some types of predominantly apical HCM. Patients with HCM present with progressive dyspnea, especially after 40-50 years, due to diastolic dysfunction. Implantable cardioverter defibrillator therapy is considered the best treatment option, particularly in patients with a history of sustained ventricular tachycardia/ventricular fibrillation, patients with extensive left ventricular involvement, and those with a history of syncope." @default.
- W4205245068 created "2022-01-25" @default.
- W4205245068 date "2021-09-17" @default.
- W4205245068 modified "2023-10-14" @default.
- W4205245068 title "Inherited Heart Diseases" @default.
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- W4205245068 doi "https://doi.org/10.1002/9781119536475.ch21" @default.
- W4205245068 hasPublicationYear "2021" @default.
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