Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Textbook 2020Latest edition Springer Nature Switzerland AG 202

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Mitochondrial Cardiomyopathiespresent in the majority of patients with cardiomyopathy, arrhythmias, and conduction defects being the most prevalent. Hypertrophic cardiomyopathy is the most frequently encountered cardiomyopathy in PMD but also dilated cardiomyopathy and left ventricular non-compaction can occur. Cardiac symptoms

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Catecholaminergic Polymorphic Ventricularclude polymorphic VT reproducibly induced during exercise test, isoproterenol infusion or emotion and exercise. CPVT occurs in children and adolescents and causes syncope and sudden cardiac death at a young age, in absence of structural heart disease. The resting electrocardiogram (ECG), including t

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https://doi.org/10.1007/978-3-642-20144-8me also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myocardial proteins to produce a final DCM phenotype. Recommendations on genetic screening and cardiac screening are provided in this chapter.