| Literature DB >> 3186348 |
M Natowicz1, J Chatten, R Clancy, K Conard, T Glauser, D Huff, A Lin, W Norwood, L B Rorke, A Uri.
Abstract
All pediatric autopsies of patients with hypoplastic left heart syndrome seen during an 11-year interval were reviewed to determine the frequency of underlying chromosomal and single-gene defects and idiopathic major extracardiac anomalies associated with this common, lethal congenital heart abnormality. Of 83 patients identified, nine had underlying chromosomal abnormalities, four had single-gene defects, ten had one or more major extracardiac anomalies without an identifiable chromosomal or mendelian disorder, and two were infants of insulin-dependent diabetic mothers. Overall, 23 patients (28%) had a genetic disorder and/or major extracardiac anomaly. The substantial prevalence of genetic causes of and major extracardiac anomalies associated with hypoplastic left heart syndrome underscores the need for a detailed genetic evaluation for all patients with hypoplastic left heart syndrome.Entities:
Mesh:
Year: 1988 PMID: 3186348
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124