| Literature DB >> 21918661 |
Paulo Rego Sousa1, Sónia Antunes, Alexandra Couto, Gonçalo Cassiano Santos, Luis Gagp Leal, Manuel Pedro Magalhães.
Abstract
Congenital sternal malformation is a rare anomaly often diagnosed as an asymptomatic condition at birth. The authors report a clinical case of a full-term female neonate with congenital sternal cleft and partial ectopia cordis. Successful surgical repair was accomplished at 6 days of age. When surgery is performed shortly after birth, the procedure is easier and better results are achieved.Entities:
Year: 2009 PMID: 21918661 PMCID: PMC3029128 DOI: 10.1136/bcr.06.2009.2018
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X