Primary endocardial fibroelastosis; a familial condition.
نویسندگان
چکیده
منابع مشابه
Heredity in primary endocardial fibroelastosis.
Twenty-six cases of endocardial fibroelastosis were collected from three hospitals in Manchester over a ten-year period. Nine cases occurred in 4 families and these are discussed in detail. X-linked recessive inheritance seems likely in one family in which two probable female carriers had subarachnoid haemorrhages. In a second family an apparently normal man produced two children with endocardi...
متن کاملThe Diagnosis of Primary Endocardial Fibroelastosis.
THE term endocardial fibroelastosis was first used by Weinberg and Himelfarbl to describe the condition of infantile cardiomegaly in which the pathologic lesion consisted of varying degrees of fibroelastotic proliferation within the endocardium. It is now well recognized that there are two forms of endocardial fibroelastosis. The first is associated with numerous congenital heart defects and ap...
متن کاملEndocardial Fibroelastosis
It is rare only 1-2% of all congenital heart diseases. The number of cases has fallen dramatically in recent years, possibly secondary to better antenatal scanning. It may be familial (10%) with a predominantly X-linked pattern. [3] It affects both sexes equally, usually presenting during the first 3-6 months of life in 80% of cases. Typical age of diagnosis is 2-12 months. It rarely is reporte...
متن کامل[Endocardial fibroelastosis].
Four children were studied in whom form of primary endocardial fibroel diagnosed clinically. In one of these diagnosis was confirmed at autopsy. In the routine clinical and laboratory cardiac catheterization and selective ography were performed on the 4 pati( angiocardiograms were taken at 6 or 1 second after automatic injection at 5 K per cent sodium diprotrizoate (Mioko main pulmonary artery....
متن کاملEndocardial Fibroelastosis
It is rare only 1-2% of all congenital heart diseases. The number of cases has fallen dramatically in recent years, possibly secondary to better antenatal scanning. It may be familial (10%) with a predominantly X-linked pattern. [3] It affects both sexes equally, usually presenting during the first 3-6 months of life in 80% of cases. Typical age of diagnosis is 2-12 months. It rarely is reporte...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1970
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.45.244.813-a