Familial hypertrophic cardiomyopathy in Ceylon.

نویسندگان

  • N J Wallooppillai
  • D P Atukorale
  • M de S Jayasinghe
  • S Kulathungam
چکیده

Forty patients had a diagnosis of hypertrophic cardiomyopathy confirmed by right and left heart catheterization or necropsy. The families of the patients were investigated and i5 of the 40 had a positive family history. In these 15families, 79 parents and sibs were alive, and 55 werefound to have evidence of the disease. Of the 55, 40 were male and i5female. Thefamilial incidence was 37.5 per cent. The sex ratio in the familial

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DIFFUSE CORONARY ARTERIAL ECTASIA WITH HYPERTROPHIC CARDIOMYOPATHY

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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 35 2  شماره 

صفحات  -

تاریخ انتشار 1973