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Diagnosing Von Willebrand Disease

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http://hdl.handle.net/10355/7675
dc.contributor.authorCrownover, Brian K.eng
dc.contributor.authorSleuwen, Leslieeng
dc.contributor.authorKetterman, Elizabetheng
dc.date.issued2010eng
dc.description.abstractThe diagnosis of vWD requires two clinical criteria: (1) a personal history, family history, or physical evidence of mucocutaneous bleeding and (2) a qualitative or quantitative decrease in functional activity of von Willebrand factor (vWF). (Strength of Recommendation [SOR]: C, based on expert opinion). Some patients with borderline decreased functional activity of vWF will meet the criteria for vWD if the other clinical criterion is present. (SOR: C, based on expert consensus and opinion).eng
dc.identifier.urihttp://hdl.handle.net/10355/7675eng
dc.languageEnglisheng
dc.publisherFamily Physicians Inquiries Networkeng
dc.relation.ispartofcollectionClinical Inquiries, 2010 (MU)eng
dc.relation.ispartofcommunityUniversity of Missouri-Columbia. School of Medicine. Department of Family and Community Medicine. Family Physicians Inquiries Networkeng
dc.relation.ispartofseriesAmerican family physician, 81, no. 12 (June 2010): 1415-1418.eng
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.eng
dc.subjectdiagnostic criteriaeng
dc.subjectbleeding disordereng
dc.subject.lcshVon Willebrand disease -- Diagnosiseng
dc.subject.lcshBlood coagulation disorderseng
dc.subject.lcshVon Willebrand factoreng
dc.titleDiagnosing Von Willebrand Diseaseeng
dc.typeArticleeng


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