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Check out the latest articles on von Willebrand disease

Last update : Thursday November 07, 2024

Severe haemorrhages leading to a diagnosis of rare bleeding disorder occur at a very young age: A study from the FranceCoag network

The occurrence of unexplained severe bleeding, especially in childhood, can be related to coagulation pathway disorders, associated or not with maltreatment. In such cases of severe bleeding or intracerebral...
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Haemophilia 2024; 30(4): 981-7
Sandrine Meunier et al.

Retrospective chart review of GI bleeding in people with von Willebrand disease

People with a severe von Willebrand disease (VWD) bleeding phenotype experience frequent, prolonged and excessive mucocutaneous bleeding, such as epistaxis, gingival or gastrointestinal (GI) bleeding,...
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Haemophilia 2024; 30(4): 970-80
Jonathan C. Roberts et al.

Bleeding management in type 3 von Willebrand disease with anti‐von Willebrand factor inhibitor: A literature review and case report

Type 3 von Willebrand disease (VWD), an inherited blood disorder, is caused by a total deficiency of von Willebrand factor (VWF), associated to very low levels of factor VIII (FVIII) [1]. Bleeding manifestations...
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eJHaem 2024; 5(5): 964-70
Aurélie Briane et al.

Patient‐reported data on the severity of Von Willebrand disease

Von Willebrand factor (VWF) has an important function in primary haemostasis by mediating the adhesion and aggregation of platelets at the site of injury. Von Willebrand disease (VWD) is caused by a deficiency of VWF and is characterized by a heterogeneous bleeding phenotype. The disease is categorized into three types: VWD with reduced VWF levels (type 1), dysfunctional VWF (type 2) or absence of VWF (type 3). The objective severity classification...
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Haemophilia 2024; AOP: 10.1111/hae.15103
Calvin B.van Kwawegen et al.

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