Familial dilated (congestive) cardiomyopathy. Occurrence in two brothers and an overview of the literature.

نویسندگان

  • J Z Przybojewski
  • J J van der Walt
  • P J van Eeden
  • F A Tiedt
چکیده

Two young White brothers had dilated (congestive) cardiomyopathy. The elder came to autopsy after a chronic course of congestive cardiac failure, the younger underwent repeated cardiac catheterization and transvenous right ventricular endomyocardial biopsy specimens demonstrated histopathological features in keeping with a diagnosis of idiopathic dilated cardiomyopathy. These brothers may have the familial form of the disease, although post-viral myocarditis cardiomyopathy cannot be entirely excluded. The literature relating to familial dilated (congestive) cardiomyopathy is reviewed.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Possible X linked congenital mitochondrial cardiomyopathy in three families.

Familial cases of childhood congestive cardiomyopathy with X linked recessive inheritance and abnormalities of heart muscle mitochondria have been previously reported. We report here three families with possible X linked congestive cardiomyopathy and specific mitochondrial abnormalities. The heart disorder presented as endocardial fibroelastosis with neonatal death in two brothers in one family...

متن کامل

Familial dilated cardiomyopathy--a case report from western Nepal.

Dilated cardiomyopathy (DCM) is a common cause of congestive cardiac failure all over the world. Most cases are idiopathic and sporadic. However, an increasing number are found to have a genetic basis which accounts for about 25.0-30.0% of cases all over the world. Different modes of inheritance and mutations have been implicated in these familial cases. Regardless of the type, they usually pre...

متن کامل

پیگیری و سرنوشت 115 کودک مبتلا به کاردیومیوپاتی اتساعی اولیه

    Background & Aim: In childhood, dilated cardiomyopathy has a prevalence of 36 in 100000. Its prognosis is one of the most important matters. The chance of 5-year survival is reported to be around 50% and 10-year one around 25%. We aimed to study the prognosis, treatment, and mortality of dilated cardiomyopathy patients in Iran. Patients & Method: In this descriptive study, the medical recor...

متن کامل

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

BACKGROUND Inherited gene defects are an important cause of dilated cardiomyopathy. Although the chromosome locations of some defects and 1 disease gene (actin) have been identified, the genetic etiologies of most cases of familial dilated cardiomyopathy remain unknown. METHODS AND RESULTS We clinically evaluated 3 generations of a kindred with autosomal dominant transmission of dilated cardi...

متن کامل

FAMILIAL COLLOID CYST OF THE THIRD VENTRICLE: A CASE REPORT AND REVIEW OF THE LITERATURE

Familial colloid cyst of the third ventricle is very rare. This is one of the two largest families reported and the first in which all affected members are siblings. One asymptomatic sister was found by screening, emphasizing the value of screening. A brother and two sisters from a family consisting of three brothers and three sisters who were diagnosed as having colloid cyst of the third v...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde

دوره 66 1  شماره 

صفحات  -

تاریخ انتشار 1984