ENDOCARDIAL FIBROELASTOSIS (EFE): MOLECULAR EVIDENCE FOR THE ROLE OF MUMPS VIRUS AS AN ETIOLOGICAL AGENT. • 124
نویسندگان
چکیده
منابع مشابه
Endocardial 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...
متن کاملEndocardial 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: Pediatric Research
سال: 1996
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-199604001-00143