Linked Life Data

17276930

Source:http://linkedlifedata.com/resource/pubmed/id/17276930

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2007-2-5
pubmed:abstractText
Interruption of the aortic arch is a rare and usually lethal congenital anomaly that is often associated with multiple cardiac malformations. Most neonates with aortic arch interruption perish once the ductus arteriosus closes after birth. However, sporadic cases have been reported to survive into adulthood uneventfully. Here, we report a 19-year-old male with a 3-month history of exertional dyspnea. A series of cardiovascular studies confirmed the presence of aortic arch interruption in conjunction with sinus venosus atrial septal defect and partial anomalous pulmonary venous connection. To the best of our knowledge, such an association has not been previously reported in adults.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1726-4901
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
30-2
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
An adult with aortic arch interruption associated with sinus venosus atrial septal defect and partial anomalous pulmonary venous connection.
pubmed:affiliation
Cardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan, R.O.C.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't