rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
1992-8-21
|
pubmed:abstractText |
Congenital aortic regurgitation is rare as an isolated lesion. We describe seven children with no physical features of the Marfan syndrome in the patients or their families and no other cardiac lesions who had congenital valvular aortic regurgitation.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0735-1097
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
20
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
366-72
|
pubmed:dateRevised |
2010-3-24
|
pubmed:meshHeading |
pubmed-meshheading:1634673-Aortic Valve,
pubmed-meshheading:1634673-Aortic Valve Insufficiency,
pubmed-meshheading:1634673-Female,
pubmed-meshheading:1634673-Follow-Up Studies,
pubmed-meshheading:1634673-Heart Valve Prosthesis,
pubmed-meshheading:1634673-Humans,
pubmed-meshheading:1634673-Infant,
pubmed-meshheading:1634673-Infant, Newborn,
pubmed-meshheading:1634673-Male,
pubmed-meshheading:1634673-Marfan Syndrome,
pubmed-meshheading:1634673-Reoperation,
pubmed-meshheading:1634673-Time Factors
|
pubmed:year |
1992
|
pubmed:articleTitle |
Congenital aortic regurgitation: natural history and management.
|
pubmed:affiliation |
Division of Pediatric Cardiology, New York Hospital-Cornell University Medical Center, New York 10021.
|
pubmed:publicationType |
Journal Article,
Case Reports
|