| Question |
Answer |
| Factor (I): Helps with the formation of a clot. |
Fibrinogen |
| Factor (II): Coverts into thrombin during coag. cascade. |
Prothrombin |
| Factor (III): Activates Factor VII when exposed to tissue fluids. |
Tissue Thromboplastin |
| Factor (IV): Assists in the activation of other factors. |
Ionized Calcium |
| Factor (V): Accelerates the conversion of Prothrombin to Thrombin. |
Proaccelerin |
| Factor (VI) |
Not assigned |
| Factor (VII): Intrinsic factor activated by Factor III. |
Proconvertin |
| Factor (VIII): Passed on from father to son, loss of this factor leads to inability to clot. |
Antihemophilic A |
| Factor (IX): Other names for this factor include Antihemophilic B and plasma thromboplastin component. |
Christmas Factor |
| Factor (X): Start of Common Pathway |
Stuart Prower |
| Factor (XI): Start of Intrinsic Pathway |
Plasma Thromboplastin Antecedent |
| Factor (XII): Activated when a foreign substance is in the body. |
Hageman Factor A.K.A. "Contact Factor" |
| Factor (XIII): Helps to further stabilize the clot. |
Fibrin Stabilizing Factor(FSF) |
| High molecular weight kininogen(HMWK) is also known as what Factor? |
Fitzgerald Factor |
| Prekallikren is also known as what Factor? |
Fletcher Factor |
| Factor V Leiden: this mutated gene leads to what? |
Increase in clot formation which results in a degradation of Factor (V), by Protein C. |
Spanish 3
