AMT MLT Exam Study Guide UPDATED ACTUAL
Questions and CORRECT Answers | A+ Verified |
2026
• What inhibits vitamin K dependent coagulation factors? -✓✓ Warfarin (oral)
• Factor VIII deficiency is also called -✓✓ Hemophilia A
• Factor IX deficiency is also called -✓✓ Hemophilia B
• What evaluates adequacy of fibrinogen in heparinized pts? -✓✓ RPR
• von Willebrand factor -✓✓ Mediate a bridge between glycoprotein complex on
platelets and collagen on sub endothelial surface (defect can cause impaired
platelet adhesion and aggregation)
• Stuart-Prower factor -✓✓ X-factor, is a part of cleaning prothrombin into
thrombin
• Hageman factor -✓✓ Factor XII, is in the intrinsic pathway, activates Fletcher
factor
• Fletcher Factor -✓✓ Pre-K in intrinsic pathway and activates factor XI
• Streptokinase -✓✓ Exogenous activator for plasminogen in fibrinolytic system
,• What is the end product of coagulation cascade? -✓✓ fibrin
• Intrinsic and common passway -✓✓ aPTT
• extrinsic and common pathways -✓✓ PT
• Average bleeding time -✓✓ 1-7min
• Common pathway factors -✓✓ X, V, II, I
• extrinsic factors -✓✓ VII
• intrinsic factors -✓✓ XII, XI, IX, VIII
• Fibrinolysis -✓✓ dissolution of a clot
• Primary homeostasis -✓✓ Formation of non-stable platelet plug
• Secondary homeostasis -✓✓ Formation of durable fibrin strand
• Most specific fibrinogen function test, not affected by heparin -✓✓ thrombin time
• Non-specific fibrinogen function test -✓✓ PT and PTT
,• VLDL -✓✓ endogenous triglycerides transport
• Chylomicrons -✓✓ exogenous triglycerides transport
• HDL and LDL -✓✓ Cholesterol transport
• adult hemoglobin -✓✓ 2 alpha and 2 beta chains
• fetal hemoglobin -✓✓ 2 alpha and 2 gamma
• Hemoglobin A2 -✓✓ 2 alpha and 2 delta
• Type I hypersensitivity -✓✓ IgE mediated
• Type II hypersensitivity -✓✓ IgG
• Type III hypersensitivity -✓✓ IgM and IgG
• Heinz bodies lead to -✓✓ G6PD deficiency
• Microangiopathic Hemolytic Anemia -✓✓ Schistocytes ceratocytes and teardrop
cells
• Abetalipoproteinemia -✓✓ Acanthocytes
, • Beta Thalassemia -✓✓ target cells (codocytes)
• Howell-Jolly bodies -✓✓ DNA
• Heinz bodies -✓✓ denatured hemoglobin
• Papperheimer bodies -✓✓ Nonferritin iron
• Dohle bodies -✓✓ Rrna in leukocytes
• Alpha thalassemia minor -✓✓ two genes are defective
• Alpha, thalassemia major -✓✓ four genes are defective
• silent carrier of alpha thalassemia -✓✓ One gene is defective
• Hemoglobin H disease -✓✓ 3 a-genes deleted
-more likely asian
• Immunoglobulin light chain consist of -✓✓ Kappa and lambda
• Serum protein can be separated by cellulose acetate electrophoresis into 5
fractions -✓✓ Albumin, alpha1 globulin, alpha2 globulin, beta globulin and delta
globulin
Questions and CORRECT Answers | A+ Verified |
2026
• What inhibits vitamin K dependent coagulation factors? -✓✓ Warfarin (oral)
• Factor VIII deficiency is also called -✓✓ Hemophilia A
• Factor IX deficiency is also called -✓✓ Hemophilia B
• What evaluates adequacy of fibrinogen in heparinized pts? -✓✓ RPR
• von Willebrand factor -✓✓ Mediate a bridge between glycoprotein complex on
platelets and collagen on sub endothelial surface (defect can cause impaired
platelet adhesion and aggregation)
• Stuart-Prower factor -✓✓ X-factor, is a part of cleaning prothrombin into
thrombin
• Hageman factor -✓✓ Factor XII, is in the intrinsic pathway, activates Fletcher
factor
• Fletcher Factor -✓✓ Pre-K in intrinsic pathway and activates factor XI
• Streptokinase -✓✓ Exogenous activator for plasminogen in fibrinolytic system
,• What is the end product of coagulation cascade? -✓✓ fibrin
• Intrinsic and common passway -✓✓ aPTT
• extrinsic and common pathways -✓✓ PT
• Average bleeding time -✓✓ 1-7min
• Common pathway factors -✓✓ X, V, II, I
• extrinsic factors -✓✓ VII
• intrinsic factors -✓✓ XII, XI, IX, VIII
• Fibrinolysis -✓✓ dissolution of a clot
• Primary homeostasis -✓✓ Formation of non-stable platelet plug
• Secondary homeostasis -✓✓ Formation of durable fibrin strand
• Most specific fibrinogen function test, not affected by heparin -✓✓ thrombin time
• Non-specific fibrinogen function test -✓✓ PT and PTT
,• VLDL -✓✓ endogenous triglycerides transport
• Chylomicrons -✓✓ exogenous triglycerides transport
• HDL and LDL -✓✓ Cholesterol transport
• adult hemoglobin -✓✓ 2 alpha and 2 beta chains
• fetal hemoglobin -✓✓ 2 alpha and 2 gamma
• Hemoglobin A2 -✓✓ 2 alpha and 2 delta
• Type I hypersensitivity -✓✓ IgE mediated
• Type II hypersensitivity -✓✓ IgG
• Type III hypersensitivity -✓✓ IgM and IgG
• Heinz bodies lead to -✓✓ G6PD deficiency
• Microangiopathic Hemolytic Anemia -✓✓ Schistocytes ceratocytes and teardrop
cells
• Abetalipoproteinemia -✓✓ Acanthocytes
, • Beta Thalassemia -✓✓ target cells (codocytes)
• Howell-Jolly bodies -✓✓ DNA
• Heinz bodies -✓✓ denatured hemoglobin
• Papperheimer bodies -✓✓ Nonferritin iron
• Dohle bodies -✓✓ Rrna in leukocytes
• Alpha thalassemia minor -✓✓ two genes are defective
• Alpha, thalassemia major -✓✓ four genes are defective
• silent carrier of alpha thalassemia -✓✓ One gene is defective
• Hemoglobin H disease -✓✓ 3 a-genes deleted
-more likely asian
• Immunoglobulin light chain consist of -✓✓ Kappa and lambda
• Serum protein can be separated by cellulose acetate electrophoresis into 5
fractions -✓✓ Albumin, alpha1 globulin, alpha2 globulin, beta globulin and delta
globulin
