Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Book 20162nd edition Springer International Publishing Switzer

官僚統(tǒng)治

rheumatology

Restrictive Cardiomyopathyof impaired diastolic filling. In the early stages, systolic function may be normal, but when the disease progresses, systolic function usually declines as well. There is an overlap with other types of cardiomyopathy, such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and left

chalice

Mitochondrial Cardiomyopathy skeletal muscles. Most of the mitochondrial diseases are caused by mutations in the nuclear DNA, but approximately 15% are caused by mutations in the mitochondrial DNA, making genetic counseling difficult. The combination of cardiomyopathy, deafness, diabetes, encephalopathy and myopathy suggests m

Cryptic

Long QT Syndromeen death. It is caused by prolongation of the repolarization phase of the cardiac action potential, which may manifest as lengthening of the heart rate-corrected QT interval (QTc) on the surface electrocardiogram (ECG). This chapter reviews the clinical presentation of LQTS, its diagnosis, and princ

繁忙

Brugada Syndromea common phenotype: resuscitated from sudden cardiac death (SCD) caused by documented ventricular fibrillation (VF), showing a characteristic ST-segment elevation in the right precordial leads (Fig. 11.1) in a structurally normal heart. Nowadays, this entity is known as Brugada Syndrome (BrS). In th

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figure

Idiopathic Ventricular Fibrillationom sudden cardiac death. To date, the IVF was defined excluding other primary electrical disorders. IVF may not be composed of a single entity but contain multiple forms by clinical manifestations and possible pathogenetic backgrounds. In this chapter, IVF can be described in two groups: the early r

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多產(chǎn)魚

內(nèi)向者

https://doi.org/10.1007/978-3-319-44203-7Hypertrophic cardiomyopathy; Short QT-syndrome; Brugada syndrome; Sudden cardiac death; Congenital heart