منابع مشابه
Right ventricular dilated cardiomyopathy.
Fourteen patients with predominantly right sided dilated cardiomyopathy were studied, of whom five died suddenly. The condition is characterised by male preponderance, syncope, ventricular tachycardia, which typically has a left bundle branch block pattern on the surface electrocardiogram, and right heart failure. The diagnosis should be considered in patients presenting with otherwise unexplai...
متن کاملFamilial right ventricular dilated cardiomyopathy.
Cardiomyopathy of unknown cause occurred in three of six siblings. The course of the illness was marked by life threatening supraventricular and ventricular arrhythmias, sinoatrial block, atrioventricular block, and embolism (in one patient). The disease was characterised by right ventricular dilatation. Two of the three patients died aged 32 and 48. No new cases of the disease were found when ...
متن کاملArrhythmogenic right ventricular dysplasia/ cardiomyopathy versus dilated right ventricular cardiomyopathy: a problematic autopsy diagnosis?
Arrhythmogenic right ventricular dysplasia-cardiomyopathy (ARVD-C) is a rare heart condition with characteristic thinning and fibroadipose tissue replacement of the myocardium of the right ventricular wall. We have seen 20 autopsy cases with morphologic features fitting the criteria of ARVD-C in our hospital in the past 5 years. The clinical characteristics of these patients were not those desc...
متن کاملRight Ventricular Non-Compaction Cardiomyopathy in Children: Brief Review Literature
Right ventricular non-compaction cardiomyopathy (RVNC) is a genetic heterogeneous cardiomyopathy. Despite the increasing number of RVNC cases, the classification and natural history of this disorder are not completely clear. Also, because the pathogenic non-compaction cannot be easily differentiated from normal trabeculations, it is usually hard to accurately measure the prevalence of RV ...
متن کاملIsolated Right Ventricular Dilated Cardiomyopathy: An Early Diagnosis
Because of an incomplete right bundle branch block, a severe right ventricular dilatation with no left ventricular cardiomyopathy was found in a 44-year-old man. Magnetic resonance and transesophageal echocardiography confirmed the finding and these tests also failed to find any potential cause. A pulmonary hemodynamic study and a coronary angiography were strictly normal. Lastly pulmonary func...
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ژورنال
عنوان ژورنال: Heart
سال: 1984
ISSN: 1355-6037
DOI: 10.1136/hrt.51.1.25