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Anatomy General anatomy 3f55899b

Congenital hypercoagulability state are seen in all of the following except

A
Protein C deficiency
B
Protein S deficiency
C
Anti phospholipid antibody syndrome
D
MTHFR gene mutation
High-Yield Explanation
Ref Robbins 8/e p123; 9/e p 123 Antiphospholipid antibodies syndrome causes hypercoagulability: primary Secondary Primary mutation of factor 5 Anti thrombin 3 deficiency Protein C and S deficiency Fibrinolysis defects Secondary Homocysteine Tissue damage MI,DIC Antiphospholipid antibodies syndrome

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