AMT MLT QUESTIONS WITH CORRECT
ANSWERS 2025
K dependent coagulation factors - CORRECT ANSWER -II, VII, IX, X
What inhibits vitamin K dependent coagulation factors? - CORRECT ANSWER -Warfarin (oral)
Factor VIII deficiency is also called - CORRECT ANSWER -Hemophilia A
Factor IX deficiency is also called - CORRECT ANSWER -Hemophilia B
What evaluates adequacy of fibrinogen in heparinized pts? - CORRECT ANSWER -RPR
von Willebrand factor - CORRECT ANSWER -
Mediate a bridge between glycoprotein complex on platelets and collagen on sub endothelial su
rface (defect can cause impaired platelet adhesion and aggregation)
Stuart-Prower factor - CORRECT ANSWER -X-
factor, is a part of cleaning prothrombin into thrombin
Hageman factor - CORRECT ANSWER -
Factor XII, is in the intrinsic pathway, activates Fletcher factor
Fletcher Factor - CORRECT ANSWER -Pre-K in intrinsic pathway and activates factor XI
Streptokinase - CORRECT ANSWER -Exogenous activator for plasminogen in fibrinolytic system
What is the end product of coagulation cascade? - CORRECT ANSWER -fibrin
,Intrinsic and common passway - CORRECT ANSWER -aPTT
extrinsic and common pathways - CORRECT ANSWER -PT
Average bleeding time - CORRECT ANSWER -1-7min
Common pathway factors - CORRECT ANSWER -X, V, II, I
extrinsic factors - CORRECT ANSWER -VII
intrinsic factors - CORRECT ANSWER -XII, XI, IX, VIII
Fibrinolysis - CORRECT ANSWER -dissolution of a clot
Primary homeostasis - CORRECT ANSWER -Formation of non-stable platelet plug
Secondary homeostasis - CORRECT ANSWER -Formation of durable fibrin strand
Most specific fibrinogen function test, not affected by heparin - CORRECT ANSWER -
thrombin time
Non-specific fibrinogen function test - CORRECT ANSWER -PT and PTT
VLDLB- CORRECT ANSWER -endogenous triglycerides transport
,Chylomicrons l- lCORRECT lANSWER l-exogenous ltriglycerides ltransport
HDL land lLDLB- lCORRECT lANSWER l-Cholesterol ltransport
adult lhemoglobin l- lCORRECT lANSWER l-2 lalpha land l2 lbeta lchains
fetal lhemoglobin l- lCORRECT lANSWER l-2 lalpha land l2 lgamma
Hemoglobin lA2 l- lCORRECT lANSWER l-2 lalpha land l2 ldelta
Type lI lhypersensitivity l- lCORRECT lANSWER l-IgE lmediated
Type lII lhypersensitivity l- lCORRECT lANSWER l-IgG
Type lIII lhypersensitivity l- lCORRECT lANSWER l-IgM land lIgG
Heinz lbodies llead lto l- lCORRECT lANSWER l-G6PD ldeficiency
Microangiopathic lHemolytic lAnemia l- lCORRECT lANSWER l-
lSchistocytes lceratocytes land lteardrop lcells
Abetalipoproteinemia l- lCORRECT lANSWER l-Acanthocytes
Beta lThalassemia l- lCORRECT lANSWER l-target lcells l(codocytes)
Howell-Jolly lbodies l- lCORRECT lANSWER l-DNA
, Heinz lbodies l- lCORRECT lANSWER l-denatured lhemoglobin
Papperheimer lbodies l- lCORRECT lANSWER l-Nonferritin liron
Dohle lbodies l- lCORRECT lANSWER l-Rrna lin lleukocytes
Alpha lthalassemia lminor l- lCORRECT lANSWER l-two lgenes lare ldefective
Alpha, lthalassemia lmajor l- lCORRECT lANSWER l-four lgenes lare ldefective
silent lcarrier lof lalpha lthalassemia l- lCORRECT lANSWER l-One lgene lis ldefective
Hemoglobin lH ldisease l- lCORRECT lANSWER l-3 la-genes ldeleted
-more llikely lasian
Immunoglobulin llight lchain lconsist lof l- lCORRECT lANSWER l-Kappa land llambda
Serum lprotein lcan lbe lseparated lby lcellulose lacetate lelectrophoresis linto l5 lfractions l-
CORRECT lANSWER l-Albumin, lalpha1 lglobulin, lalpha2 lglobulin, lbeta lglobulin land ldelta lglobulin
Acutr lhemolytic ltransfusion lrxn l- lCORRECT lANSWER l-
lHemoglobinemia, lhemoglobinuria, lhypertension
Hemoglobinuria l- lCORRECT lANSWER l-excess lhemoglobin lin lurine
adult lbone lmarrow lred lcells lmost labundant l- lCORRECT lANSWER l-Metamyelo l(3-20%)
ANSWERS 2025
K dependent coagulation factors - CORRECT ANSWER -II, VII, IX, X
What inhibits vitamin K dependent coagulation factors? - CORRECT ANSWER -Warfarin (oral)
Factor VIII deficiency is also called - CORRECT ANSWER -Hemophilia A
Factor IX deficiency is also called - CORRECT ANSWER -Hemophilia B
What evaluates adequacy of fibrinogen in heparinized pts? - CORRECT ANSWER -RPR
von Willebrand factor - CORRECT ANSWER -
Mediate a bridge between glycoprotein complex on platelets and collagen on sub endothelial su
rface (defect can cause impaired platelet adhesion and aggregation)
Stuart-Prower factor - CORRECT ANSWER -X-
factor, is a part of cleaning prothrombin into thrombin
Hageman factor - CORRECT ANSWER -
Factor XII, is in the intrinsic pathway, activates Fletcher factor
Fletcher Factor - CORRECT ANSWER -Pre-K in intrinsic pathway and activates factor XI
Streptokinase - CORRECT ANSWER -Exogenous activator for plasminogen in fibrinolytic system
What is the end product of coagulation cascade? - CORRECT ANSWER -fibrin
,Intrinsic and common passway - CORRECT ANSWER -aPTT
extrinsic and common pathways - CORRECT ANSWER -PT
Average bleeding time - CORRECT ANSWER -1-7min
Common pathway factors - CORRECT ANSWER -X, V, II, I
extrinsic factors - CORRECT ANSWER -VII
intrinsic factors - CORRECT ANSWER -XII, XI, IX, VIII
Fibrinolysis - CORRECT ANSWER -dissolution of a clot
Primary homeostasis - CORRECT ANSWER -Formation of non-stable platelet plug
Secondary homeostasis - CORRECT ANSWER -Formation of durable fibrin strand
Most specific fibrinogen function test, not affected by heparin - CORRECT ANSWER -
thrombin time
Non-specific fibrinogen function test - CORRECT ANSWER -PT and PTT
VLDLB- CORRECT ANSWER -endogenous triglycerides transport
,Chylomicrons l- lCORRECT lANSWER l-exogenous ltriglycerides ltransport
HDL land lLDLB- lCORRECT lANSWER l-Cholesterol ltransport
adult lhemoglobin l- lCORRECT lANSWER l-2 lalpha land l2 lbeta lchains
fetal lhemoglobin l- lCORRECT lANSWER l-2 lalpha land l2 lgamma
Hemoglobin lA2 l- lCORRECT lANSWER l-2 lalpha land l2 ldelta
Type lI lhypersensitivity l- lCORRECT lANSWER l-IgE lmediated
Type lII lhypersensitivity l- lCORRECT lANSWER l-IgG
Type lIII lhypersensitivity l- lCORRECT lANSWER l-IgM land lIgG
Heinz lbodies llead lto l- lCORRECT lANSWER l-G6PD ldeficiency
Microangiopathic lHemolytic lAnemia l- lCORRECT lANSWER l-
lSchistocytes lceratocytes land lteardrop lcells
Abetalipoproteinemia l- lCORRECT lANSWER l-Acanthocytes
Beta lThalassemia l- lCORRECT lANSWER l-target lcells l(codocytes)
Howell-Jolly lbodies l- lCORRECT lANSWER l-DNA
, Heinz lbodies l- lCORRECT lANSWER l-denatured lhemoglobin
Papperheimer lbodies l- lCORRECT lANSWER l-Nonferritin liron
Dohle lbodies l- lCORRECT lANSWER l-Rrna lin lleukocytes
Alpha lthalassemia lminor l- lCORRECT lANSWER l-two lgenes lare ldefective
Alpha, lthalassemia lmajor l- lCORRECT lANSWER l-four lgenes lare ldefective
silent lcarrier lof lalpha lthalassemia l- lCORRECT lANSWER l-One lgene lis ldefective
Hemoglobin lH ldisease l- lCORRECT lANSWER l-3 la-genes ldeleted
-more llikely lasian
Immunoglobulin llight lchain lconsist lof l- lCORRECT lANSWER l-Kappa land llambda
Serum lprotein lcan lbe lseparated lby lcellulose lacetate lelectrophoresis linto l5 lfractions l-
CORRECT lANSWER l-Albumin, lalpha1 lglobulin, lalpha2 lglobulin, lbeta lglobulin land ldelta lglobulin
Acutr lhemolytic ltransfusion lrxn l- lCORRECT lANSWER l-
lHemoglobinemia, lhemoglobinuria, lhypertension
Hemoglobinuria l- lCORRECT lANSWER l-excess lhemoglobin lin lurine
adult lbone lmarrow lred lcells lmost labundant l- lCORRECT lANSWER l-Metamyelo l(3-20%)
