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Von Willebrand's disease (comparison with the features of Haemophilia A and Haemophilia B)

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Comparison between the clinical and laboratory features found in Haemophilia A, Haemophilia B and Von Willebrand's disease

Haemophilia A

Haemophilia B

Von Willebrand's disease

Mode of inheritance

X-linked

X-linked

Autosomal Dominant (incomplete)

Main sites of Bleeding

muscle, joints, following trauma or post operation

muscle, joints, following trauma or post operation

skin cuts, mucous membranes, following trauma and post operation

platelets

normal platelet count

normal platelet count

normal platelet count

bleeding time

normal

normal

prolongation of bleeding time

prothrombin time

normal

normal

normal

Activated partial thromboplastin time (APTT)

prolonged

prolonged

prolonged

von Willebrand's Factor

normal

normal

reduced levels

factor VIII

low levels

normal

low levels - vWF is the carrier molecule for factor VIII thus preventing it from premature destruction - this property explains the reduced factor VIII levels found in von Willebrands disease

factor IX

normal

low levels

low levels

ristocetin-induced platelet aggregation

normal

normal

ristocetin fails to induce platelet aggregation in von Willebrand's patients because of lack of vWF:R - a cofactor for ristocetin


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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