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PMID: 9843040 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Population-based study of congenital heart defects in Down syndrome.

American journal of medical genetics ·Vol. 80 ·No. 3 ·1998-11-16 ·Pages 213-7

Freeman SB, Taft LF, Dooley KJ, Allran K, Sherman SL, Hassold TJ, Khoury MJ, Saker DM

Abstract

Mental retardation and hypotonia are found in virtually all Down syndrome (DS) individuals, whereas congenital heart defects (CHDs) are only present in a subset of cases. Although there have been numerous reports of the frequency of CHDs in DS, few of the studies have had complete ascertainment of DS in a defined geographic area. The Atlanta Down Syndrome Project, a population-based study of infants born with trisomy 21, provides such a resource. In the first 6.5 years of the study, 243 trisomy 21 livebirths were identified in the five-county Atlanta area (birth prevalence: 9.6/10,000). Cardiac diagnoses were available on 227 (93%) of the cases and 89% of these evaluations were made by echocardiography, cardiac catheterization, surgery, or autopsy. Of the 227 DS infants, 44% had CHDs including 45% atrioventricular septal defect (with or without other CHDs), 35% ventricular septal defect (with or without other CHDs), 8% isolated secundum atrial septal defect, 7%, isolated persistent patent ductus arteriosus, 4% isolated tetralogy of Fallot, and 1% other. This report is unique in that it contains the largest number of trisomy 21 infants ascertained in a population-based study where modern techniques for diagnosing cardiac abnormalities predominate.

MeSH Terms
Down Syndrome/physiopathology Heart Defects, Congenital Humans Infant, Newborn
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Freeman S B
Department of Genetics, Emory University, Atlanta, Georgia 30322, USA. [email protected]
Taft L F
Dooley K J
Allran K
Sherman S L
Hassold T J
Khoury M J
Saker D M
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1998-11-16
Pages
213-7
Language
English
Region
United States
NLM ID
7708900
Subset
IM
Grants
NICHD NIH HHS · N01-HD 92907 · United States
NICHD NIH HHS · P01-HD 32111 · United States
Corrections
CommentIn
External Links
PubMed source
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