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Hemostasis

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Question
Answer
Pupura   abnormal bleeding.  
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Wiskott-Aldrch syndrome   Smallest platelets seen  
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May-Hegglin anomaly   large platelets  
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Alports syndrome (hereditary)   Giant platelets and thrombocytopenia  
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Bernard-Soulier syndrome   largest platelets seen . Autosomal bleeding disorder, missing platelets glycoproteins  
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Increased utilization of platelets   intravascular coagulation,vascular injury, DIC, Trauma  
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Severe Liver disease   Decreased fibrinogen levels,Prolonged PT  
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Hemophilia A   Inherited. Factor 8 functionally inactive. Impairs coagulation ability. Male sex linked.  
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VonWillebrand Disease   Acquired. Associated with Lupus.prolonged bleeding times.  
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DIC   complication or result of other diseases. d dimer, pt, aptt all increased  
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Antithrombin III   Inhibits thrombin. Protease inhibitor.  
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Heparin Cofactor   inhibits thrombin.  
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Protein C   Major blood coagulation regulatory . Vit k dependent  
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APTT Activated Partial Thromboplastin Time   time required to make thrombin and fibrin polymers. Normal less then 35 sec Evulates XII,XI,VII,X,V,II and II using intrinsic  
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PT Prothrombin Time   Time required to generate thrombin and fibrin using extrinsic. Thromboplastin and Ca2+. Evulates VII,X,V,II or I  
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INR International Normal Ratio   Standardize the difference in sensitivity of thromboplastin reagents and the effects on PT assays  
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INR Ratio   INR= (PT/mean normal pro time)  
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Created by: Kateskate
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