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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2008-6-3
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pubmed:abstractText |
The diagnosis of Marfan syndrome (MFS) is usually initially based on clinical criteria according to the number of major and minor systems affected following international nosology. The number of FBN1 mutation carriers, at risk of aortic complications who would not be properly diagnosed based only on clinical grounds, is of growing importance owing to the increased availability of molecular screening. The aim of the study was to identify patients who should be considered for FBN1 mutation screening.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1468-6244
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pubmed:author |
pubmed-author:AdèsLL,
pubmed-author:ArbustiniEE,
pubmed-author:Arslan-KirchnerMM,
pubmed-author:BeroudCC,
pubmed-author:BinquetCC,
pubmed-author:BoileauCC,
pubmed-author:Bonithon-KoppCC,
pubmed-author:CallewaertBB,
pubmed-author:ChikuSS,
pubmed-author:ClaustresMM,
pubmed-author:Collod-BeroudGG,
pubmed-author:ComeglioPP,
pubmed-author:CouckePP,
pubmed-author:De BackerJJ,
pubmed-author:De PaepeAA,
pubmed-author:FaivreLL,
pubmed-author:FranckeUU,
pubmed-author:GautierEE,
pubmed-author:HallidayDD,
pubmed-author:JondeauGG,
pubmed-author:KiotsekoglouAA,
pubmed-author:LoeysB LBL,
pubmed-author:MarzilianoNN,
pubmed-author:MayerKK,
pubmed-author:PlauchuHH,
pubmed-author:RobinsonP NPN,
pubmed-author:StheneurCC
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
384-90
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pubmed:meshHeading |
pubmed-meshheading:18310266-Adolescent,
pubmed-meshheading:18310266-Adult,
pubmed-meshheading:18310266-Aged,
pubmed-meshheading:18310266-Aorta,
pubmed-meshheading:18310266-Child,
pubmed-meshheading:18310266-Female,
pubmed-meshheading:18310266-Humans,
pubmed-meshheading:18310266-International Cooperation,
pubmed-meshheading:18310266-Male,
pubmed-meshheading:18310266-Marfan Syndrome,
pubmed-meshheading:18310266-Microfilament Proteins,
pubmed-meshheading:18310266-Mutation
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pubmed:year |
2008
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pubmed:articleTitle |
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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