Document Detail


Autosomal dominant atrial septal defect of ostium secundum type. Report of three families.
MedLine Citation:
PMID:  1952784     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The authors report on three Sicilian families with 17 individuals (10 females and 7 males) in successive generations affected by atrial septal defect of ostium secundum type (S-ASD) without conduction defect. The anomaly was inherited as an autosomal dominant trait. Cytoplasmic inheritance could be excluded, the anomaly being transmitted also by fathers. Familial S-ASD is probably more frequent than commonly reported since cardiological examination of the relatives is not routinely performed in every case of apparently sporadic ASD.
Authors:
S Li Volti; G Distefano; R Garozzo; M G Romeo; P Sciacca; F Mollica
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Annales de génétique     Volume:  34     ISSN:  0003-3995     ISO Abbreviation:  Ann. Genet.     Publication Date:  1991  
Date Detail:
Created Date:  1991-12-04     Completed Date:  1991-12-04     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0370562     Medline TA:  Ann Genet     Country:  FRANCE    
Other Details:
Languages:  eng     Pagination:  14-8     Citation Subset:  IM    
Affiliation:
Institutes of Pediatric Department, University of Catania, Italy.
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Child
Child, Preschool
Female
Genes, Dominant
Heart Murmurs / diagnosis,  etiology,  genetics
Heart Septal Defects, Atrial / diagnosis,  genetics*
Humans
Male
Middle Aged
Pedigree
Sicily

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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