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Pathology Bleeding disorder 2bfa673b

Patient with hemophilia A have bleeding disorder because of:

A
Lack of platelet aggregation
B
Lack of reaction accelerator during activation of factor X in coagulation cascade
C
Neutralization of antithrombin III
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 -Intrinsic Pathway affected -Factor VIIIa complex is the most impoant activator of factor X required for conversion of prothrombin to thrombin. -In symptomatic cases there is a tendency toward easy bruising and massive hemorrhage after trauma or operative procedures

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