Which of the following is/are true regarding inherited thrombophilia?
A) The majority of people who carry heterozygous mutations that have been associated with thrombosis do not manifest a thrombotic disease.
B) Activated protein C resistance, protein C deficiency, protein S deficiency, and antithrombin deficiency are all examples of inherited thrombophilic disorders.
C) Prothrombin nucleotide G20210A mutation, hyperhomocysteinemia, and some forms of dysfibrinogenemia are associated with thrombotic disease.
D) A and B only
E) A, B, and C
Correct Answer:
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Q13: Thrombin binds to platelets at low concentration
Q14: Which of the following is not a
Q15: Physiologic activation of plasminogen by the extrinsic
Q16: Why is thrombogenesis greatly accelerated by the
Q17: Activated protein C (APC):
A) Cleaves and inactivates
Q19: Physiologic fibrinolysis results in the proteolytic degradation
Q20: The central reaction in the fibrinolytic system
Q21: Which of the following statements about hyperhomocysteinemia
Q22: Which type of protein C deficiency is
Q23: Which autosomal dominant thrombotic disorder is associated
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