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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2004-4-28
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pubmed:abstractText |
We report the case of a long-standing female blood donor whose blood donation was processed for cryoprecipitate. The cryoprecipitate unit was chosen at random for FVIII:C estimation as part of the quality control, and a low FVIII:C level was identified. The cause of this was subsequently shown to be the Normandy variant of type-2 von Willebrand's disease due to a homozygous Arg854Gln mutation in the von Willebrand factor gene.
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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 |
Apr
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pubmed:issn |
0958-7578
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
181-4
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:15113383-Blood Component Transfusion,
pubmed-meshheading:15113383-Blood Donors,
pubmed-meshheading:15113383-Factor VIII,
pubmed-meshheading:15113383-Female,
pubmed-meshheading:15113383-Fibrinogen,
pubmed-meshheading:15113383-Homozygote,
pubmed-meshheading:15113383-Humans,
pubmed-meshheading:15113383-Middle Aged,
pubmed-meshheading:15113383-Mutation, Missense,
pubmed-meshheading:15113383-Partial Thromboplastin Time,
pubmed-meshheading:15113383-Quality Control,
pubmed-meshheading:15113383-von Willebrand Diseases
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pubmed:year |
2004
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pubmed:articleTitle |
Unconventional diagnosis of Normandy-type von Willebrand's disease in a blood donor.
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pubmed:affiliation |
Sheffield Haemophilia and Thrombosis Centre, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, UK.
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pubmed:publicationType |
Journal Article,
Case Reports
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