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Pathology General 7fa27c10

Patient with hemophilia A have bleeding disorder because of

A
Lack of platelet count
B
Lack of platelet adhesion
C
Lack of factor VIII a during activation of factor X in coagulation coscade
D
Release of thromboxane A2
High-Yield Explanation
Hemophilia A X - linked disorder 90% cases - deficiency of factor 8 10% cases functional defect of factor 8 Factor VIII a complex is the most important activator of factor X required for conversion of prothrombin to thrombin.

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