Hypertrophic cardiomyopathy with unusual features in a family.
نویسندگان
چکیده
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 infundibular pulmonary stenosis was found in two. Ischaemic heart disease was closely mimicked and it is suggested that some cases of angina with normal coronary arteriograms
منابع مشابه
Apical Hypertrophic Cardiomyopathy in a Case with Chest Pain and Family History of Sudden Cardiac Death: A Case Report
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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عنوان ژورنال:
- British heart journal
دوره 33 1 شماره
صفحات -
تاریخ انتشار 1971