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Abstract
Desmoglein-2 mutations in arrhythmogenic cardiomyopathy produce myocyte ventricular hypertrophy due to necrosis and severe calcification. This study aimsto investigate the presence of electrocardiographic signs of right ventricular hypertrophy
in patients with desmoglein-2 mutations.
Keywords
Arrhythmogenic cardiomyopathy, Desmoglein-2, Necrosis, Calcification
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OPINION
The causes of regional hypo-, a- or dyskinesis of left ventricular function in takotsubo
cardiomyopathy remains unclear. These changes are transient in many cases, but a
chronic takotsubo cardiomyopathy exist in a few cases [1].
Keywords
Myocardial Bridging, Takotsubo Cardiomyopathy, LAD
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Abstract
DAortic diseases and their complications are related to high mortality. Genetic disorders of the elastic components of the aorta (elasthopaties) cause earlier manifestation and worse prognosis of the aortic pathology among the affected subjects. Early diagnosis of such genetic disorders can lead to better control and preventive medical and surgical treatment in order to prevent complications and
improve prognosis.
Keywords
Osteogenesis imperfect, Marfan syndrome, Turner's syndrome
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