Inherited Abnormalities of Coagulation Hemophilia, von Willebrand Disease, and Beyond
Bleeding disorders are broadly classified into primary and secondary hemostatic defects
(Fig. 1).
Pediatr Clin N Am 60
Bleeding disorders are broadly classified into primary and secondary hemostatic defects
(Fig. 1).
Pediatr Clin N Am 60
מחלת וון וויליברנד היא מחלת הדמם התורשתית השכיחה ביותר, המתבטאת בדימום בעור ובריריות. חומרת הדמם משתנה מחולה לחולה ומבן משפחה אחד
Type 2B von Willebrand disease (VWD) is an inherited bleeding disorder caused by changes in von Willebrand factor (VWF)
Disseminated intravascular coagulation (DIC) is a condition characterized by systemic activation of coagulation, potentially leading to thrombotic obstruction of
Situations that ordinarily necessitate consideration of anticoagulation, such as arterial and venous thrombotic events and prevention of stroke in atrial fibrillation, become
Acquired thrombotic thrombocytopenic purpura (TTP) is characterized by thrombocytopenia and microangiopathic hemolytic anemia (MAHA) without an obvious
cause, and may
Type 2 von Willebrand disease (VWD) includes a wide range of qualitative abnormalities of von Willebrand factor structure and function resulting
This is a single guideline replacing two separate guidelines on diagnosis and management respectively, published in 2004 (Laffan et al, 2004;
A United Kingdom Haemophilia Centre Doctors’ Organization guideline on behalf of the British Committee for Standards in Haematology
Hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP)
are 2 rare clinical entities.
Pediatr Clin N Am
נותנות החסות לאיגוד:
הכניסה לאתר מותרת אך ורק לרופאים/ות בעלי רישיון לעסוק ברפואה בישראל
ו/או בעלי רישיון לעסוק ברוקחות ו/או אדם הנמנה על צוות רפואי או מחקר ביו-רפואי.