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Consulte los últimos artículos sobre la enfermedad de von Willebrand

Última actualización: Jueves, 03 de abril de 2025

Challenges and considerations of genetic testing in von Willebrand disease

von Willebrand disease (VWD) is the most common inherited bleeding disorder characterized by defects in the quantity or function of the von Willebrand factor (VWF). The diagnosis of VWD is complex, requiring...
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Research and Practice in Thrombosis and Haemostasis 2025; 9(1): 102686
Seidizadeh, Omid et al.

Etiology and diagnosis of heavy menstrual bleeding among adolescent and adult patients: a systematic review and meta-analysis of the literature

Heavy menstrual bleeding (HMB) is excessive menstrual blood loss that interferes with an individual’s quality of life. Many individuals with HMB are inadequately managed by health care providers....
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Journal of Thrombosis and Haemostasis 2025; 23(3): 863-76
Comishen, Kyle J. et al.

Von Willebrand Disease and Angiodysplasia: a wider view of pathogenesis in pursuit of therapy.

Bleeding in the GI tract continues to pose a therapeutic challenge for clinicians in patients with Von Willebrand Disease (VWD). It is associated with significant morbidity and mortality and represents...
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Haematologica 2024 Nov
Crossette-Thambiah Christina et al.

2025 Clinical Trials Update on Hemophilia, VWD, and Rare Inherited Bleeding Disorders

Clinical trial programs for inherited bleeding disorders feature an array of innovative prophylaxis options: engineered clotting factor concentrates, FVIIIa mimetics, gene therapies, and biologics to bolster thrombin generation (rebalancing agents). Increasingly, non-hemophilia bleeding disorders and a broader demographic (females, children, and infants) are being incorporated into study populations. Ongoing clinical trials broadly address three themes:...
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Am J Hematol. 2025
Jiang et al.

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