Hypertrophic cardiomyopathy with unusual features in a family.
نویسندگان
چکیده
منابع مشابه
Hypertrophic cardiomyopathy with unusual features in a family.
waves, a systolic ejection murmur, and wide splitting of the second heart sound. The electrocardiogram was characterized by a short PR interval, increasedQRS amplitude, and persistent ST depression. There was little or no cardiomegaly but some pulmonary artery prominence. There was no evidence of subaortic stenosis or coronary artery disease in three members who were catheterized, but mild infu...
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Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...
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Four members of a family with scapuloperoneal syndrome were examined and investigated. The pattern of inheritance was autosomal dominant and the myopathic basis of the muscle atrophy was established by histological studies of muscle and spinal cord. The family illustrates an unusual combination of features which appear to be distinct from those of other families with myopathic scapuloperoneal s...
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An unusual type of hypertrophic cardiomyopathy was diagnosed in a 17-year-old girl who presented with dyspnea on exertion. The hypertrophied myocardium was localized to the anterior portion of the left ventricle from the base to the apex without left ventricular outflow tract obstruction. On cardiac magnetic resonance imaging (MRI), patchy and linear delayed hyperenhancement was shown in the an...
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ژورنال
عنوان ژورنال: Heart
سال: 1971
ISSN: 1355-6037
DOI: 10.1136/hrt.33.1.55