Source:http://linkedlifedata.com/resource/pubmed/id/17370733
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
97
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pubmed:dateCreated |
2007-3-20
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pubmed:abstractText |
The von Willebrand factor plays an important role in primary and secondary hemostasis. Von Willebrand disease is due to a quantitative or qualitative abnormality of von Willebrand factor. It is the most frequent constitutional abnormality of hemostasis. The main manifestation of von Willebrand disease is a mucocutaneous hemorrhagic syndrome; however, von Willebrand disease is characterized by an important clinical and biological heterogeneity. Its transmission is autosomal, usually dominant. A screening can be made by a general practitioner on the basis of a good clinical history. It is then important to confirm the diagnosis in a specialized laboratory because an adequate treatment can be prescribed to avoid hemorrhagic complications, in particular at the time of surgical procedures.
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pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1660-9379
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
346-50
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading | |
pubmed:year |
2007
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pubmed:articleTitle |
[Von Willebrand disease: a common and unrecognized bleeding disorder].
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pubmed:affiliation |
Unité d'hémostase, HUG, Genève. francoise.boehlen@hcuge.ch
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pubmed:publicationType |
Journal Article,
English Abstract,
Review
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