Acquired inhibitors to coagulation factors other than factor VIII are extremely rare. We describe a case of a 59-year-old woman with abnormal bleeding, diagnosed with concurrent inhibitor antibodies to factor VIII and IX by Bethesda testing. We demonstrate that anti-FVIII antibodies of a very high titre are capable of disturbing the aPTT-based Bethesda assay, resulting in falsely-positive antibodies to factor IX. The case also illustrates the usefulness of the immunological assay (ELISA) in complementing the inhibitor diagnosis
Acquired hemophilia A (AHA) is a blood clotting disorder caused by the presence of autoantibodies (i...
Acquired haemophilia A is rare, autoimmune bleeding disorder caused by the production of autoantibod...
Factor VIII (FVIII) is a co-factor in the haemostatic system required for fibrin-rich clot formation...
An 88-year-old female was admitted with autoimmune hemolytic anemia (AIHA). Coagulation test reveale...
Acquired inhibitors of coagulation are antibodies that either inhibit the activity or increase the c...
Diagnose and manage the presence of factor VIII inhibitor. CASE: We present the case of a 76-year-ol...
Autoantibodies that inhibit the coagulant activity of factor VIII cause acquired haemophilia, one of...
Introduction:Accurate diagnosis of an inhibitor, a neutralizing antibody to infused factor VIII (FVI...
Item does not contain fulltextAcquired hemophilia A is a rare but severe autoimmune bleeding disorde...
The causes of an isolated prolonged activated partial thromboplastin time (APTT) with a normal proth...
Acquired hemophilia is a rare but severe condition, which is unknown to medical specialties outside ...
Acquired hemophilia A is a rare, but devastating bleeding disorder caused by spontaneous development...
Poster presented at the International Society on Thrombosis and Haemostasis 2015 Congress, 20-25 Jun...
Acquired hemophilia A is an uncommon but potentially life-threatening hemorrhagic disorder caused by...
INTRODUCTION: Deficiency or absence of factor VIII or factor IX causes hemophilia A and hemophilia ...
Acquired hemophilia A (AHA) is a blood clotting disorder caused by the presence of autoantibodies (i...
Acquired haemophilia A is rare, autoimmune bleeding disorder caused by the production of autoantibod...
Factor VIII (FVIII) is a co-factor in the haemostatic system required for fibrin-rich clot formation...
An 88-year-old female was admitted with autoimmune hemolytic anemia (AIHA). Coagulation test reveale...
Acquired inhibitors of coagulation are antibodies that either inhibit the activity or increase the c...
Diagnose and manage the presence of factor VIII inhibitor. CASE: We present the case of a 76-year-ol...
Autoantibodies that inhibit the coagulant activity of factor VIII cause acquired haemophilia, one of...
Introduction:Accurate diagnosis of an inhibitor, a neutralizing antibody to infused factor VIII (FVI...
Item does not contain fulltextAcquired hemophilia A is a rare but severe autoimmune bleeding disorde...
The causes of an isolated prolonged activated partial thromboplastin time (APTT) with a normal proth...
Acquired hemophilia is a rare but severe condition, which is unknown to medical specialties outside ...
Acquired hemophilia A is a rare, but devastating bleeding disorder caused by spontaneous development...
Poster presented at the International Society on Thrombosis and Haemostasis 2015 Congress, 20-25 Jun...
Acquired hemophilia A is an uncommon but potentially life-threatening hemorrhagic disorder caused by...
INTRODUCTION: Deficiency or absence of factor VIII or factor IX causes hemophilia A and hemophilia ...
Acquired hemophilia A (AHA) is a blood clotting disorder caused by the presence of autoantibodies (i...
Acquired haemophilia A is rare, autoimmune bleeding disorder caused by the production of autoantibod...
Factor VIII (FVIII) is a co-factor in the haemostatic system required for fibrin-rich clot formation...