Isolated ventricular non-compaction of myocardium is an unclassified cardiomyopathy with an underlying mechanism of a morphogenetic abnormality involving an arrest of compaction of the loose myocardial meshwork during fetal ontogenesis. The diagnosis of this unusual condition can be readily mistaken for idiopathic dilated cardiomyopathy and it should be considered in evaluation of patients with...

A workshop was convened on the topic of Cardiomyopathy associated with Muscular Dystrophy in Tucson, Arizona, 28–30 September 2003, sponsored by the Muscular Dystrophy Association. Workshop participants from North America, Europe and Australia set as goals to understand the pathologic basis of cardiomyopathy associated with muscular dystrophy and to review treatment strategies for cardiomyopath...

We present what may be the first documented case of takotsubo cardiomyopathy following a thoracic epidural steroid injection. The 77-year-old patient had many risk factors predisposing her to takotsubo cardiomyopathy, including gender, postmenopausal status, and numerous recent stressful events in her life. Although she presented to the emergency department with symptoms of an acute myocardial ...

Takotsubo cardiomyopathy, also known as stress-induced is a temporary left ventricular dysfunction caused by catecholamine surge under severe stress. It's characterized chest pain, non-specific ECG changes, and apical ballooning observed during catheterization. We present case of 59-year-old postmenopausal female with past medical history asthma who arrived at the ED complaining pain following ...

Takotsubo cardiomyopathy, also known as stress-induced cardiomyopathy, is a disease in which the patient exhibits transient, reversible left ventricular dysfunction that is triggered by physical or emotional stress. Prolongation of QT interval, a risk factor for arrhythmia and sudden death, has been reported to be prevalent among patients with Takotsubo cardiomyopathy and is also observed in th...

Cardiomyopathy is a disease of the heart muscle leading to abnormal structure or function in the absence of coronary artery disease, hypertension, or valvular or congenital heart disease. Currently, cardiomyopathy is the leading diagnosis of heart transplant patients worldwide. Incorporation of next-generation sequencing strategies will likely revolutionize genetic testing in cardiomyopathy. Th...

An 8-year-old girl died suddenly without prior symptoms. Post-mortem examination identified both systemic group A streptococcal infection and hypertrophic cardiomyopathy. She had no history of cardiac symptoms and was not in a high-risk group for sudden death due to hypertrophic cardiomyopathy. We believe the disseminated but asymptomatic group A streptococcal infection precipitated her early d...

The BIO14.6 hamster is a widely used model for autosomal recessive cardiomyopathy. These animals die prematurely from progressive myocardial necrosis and heart failure. The primary genetic defect leading to the cardiomyopathy is still unknown. Recently, a genetic linkage map localized the cardiomyopathy locus on hamster chromosome 9qa2.1-b1, excluding several candidate genes. We now demonstrate...

Takotsubo cardiomyopathy is very rare in the paediatric population and has not been described in a single-ventricle patient yet. We report the case of a 4-year old boy with a history of Takotsubo cardiomyopathy in whom we performed a Fontan operation. After coil embolization of the minor aortopulmonary collateral arteries, the patient developed Takotsubo cardiomyopathy. His cardiac function lar...

hypertrophic cardiomyopathy’ by DDD pacing. Third, despite the fact that the patients were mainly in New York Heart Association functional class IV before DDD pacing, in both types of cardiomyopathy a considerable increase in exercise capability is achieved.h’ Moreover, in both conditions the beneficial effects of chronic DDD pacing continue to be evident when pacing is abruptly stopped.’" Duri...