Source:http://linkedlifedata.com/resource/pubmed/id/17292616
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-3-19
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pubmed:abstractText |
Ruptured aortic root aneurysm is very rare in children less than 10 years of age. Isolated dilatation of the ascending aorta and/or aortic root in a child is mostly associated with Marfan's syndrome, and the standard surgical treatment is aortic root replacement with a composite valve graft or homograft. We report here a successful emergent T. David-V operation using two grafts of different sizes for a ruptured aortic root aneurysm in a 9-year-old child with Marfan's syndrome.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1010-7940
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
744-6
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pubmed:meshHeading |
pubmed-meshheading:17292616-Aorta,
pubmed-meshheading:17292616-Aortic Rupture,
pubmed-meshheading:17292616-Child,
pubmed-meshheading:17292616-Dilatation, Pathologic,
pubmed-meshheading:17292616-Echocardiography,
pubmed-meshheading:17292616-Humans,
pubmed-meshheading:17292616-Male,
pubmed-meshheading:17292616-Marfan Syndrome,
pubmed-meshheading:17292616-Vascular Surgical Procedures
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pubmed:year |
2007
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pubmed:articleTitle |
Emergent David-V operation for a ruptured aortic root aneurysm in a 9-year-old child.
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pubmed:affiliation |
Department of Cardiovascular Surgery, Fukui Cardiovascular Center, Shinbo 2-228 Fukui, Japan. ayak0511@yahoo.co.jp
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pubmed:publicationType |
Journal Article,
Case Reports
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