MMSC 423 HEMATOLOGY ACTUAL EXAM
PAPER 2026 FULL QUESTIONS AND
CORRECT ANSWERS GRADED A+
●● in this sex-linked recessive disorder, a common clinical finding is
hemarthrosis, normal platelet count, normal RIPA. Answer: hemophilia
A
●● In this type of vWD, pt count is normal, PTT is prolonged, vwF
antigen is very low or absent, RIPA is absent and all vWF multimers are
absent:. Answer: type 3
●● which of the following is recognized as viable treatment for TTP.
Answer: plasma exchange
●● all of the following may be seen in HUS. Answer: decreased
reticulocyte count
●● all of the following are associated with HELLP syndrome except:.
Answer: absence of schistocytes
●● In this rare recessive disorder, patients are missing the radius bone
and present with an elevated WBC count and decreased platelet count.
Answer: TAR syndrome
,●● In this syndrome platelets are lacking dense granules, and present
with oculocutaneous albinism, bleeding gums, and excessive bleeding
after surgery:. Answer: hermansky-pullak
●● which TEG parameter should let the clinical know a platelet
transfusion is indicated. Answer: decreased MA
●● in this autosomal disorder clot extraction is abnormal. Answer:
glanzmanns thromboasthenia
●● what is considered normal range for bleeding time. Answer: 2-9
minutes
●● which of the following disorders charactered by lack of alpha
granules. Answer: gray platelet
●● test measured for platelet plug to occlude the area. Answer: PFA-100
●● When running TEG, what reagent will be unemployed in the test
system for a pt on unfractionated heparin?. Answer: Heparinase
●● all of the following coagulation factor are measured in the
prothrombin complex time test except. Answer: Factor 13 (XIII)
,●● what does ISI stand for. Answer: international sensitivity index
●● all of the following are measured by the APTT except. Answer:
Factor 7 (VII)
●● This screening test for factor V involves adding a standard amount of
activated protein C for both patient plasma and normal plasma. Answer:
APTT
●● what test is elevated in uncompensated DIC. Answer: d-dimer
●● light transmittance is increased in platelet aggregation studies where
the platelet agonist employed is ADP. Answer: true
●● Patients who have deficiency in GP1B have a deficiency in adhesion.
Answer: true
●● oral anticoagulant. Answer: vitamin k
●● which of the following is decreased in uncompensated DIC. Answer:
fibrinogen
●● DDVAP is an effective treatment of. Answer: vWD type 1
, ●● what would mixing studies reveal in a patient with an inhibitor to
factor VIII. Answer: APPTT would not correct with absorbed plasma or
normal plasma
●● which of the following tests is increased in a patient with severe
hemophilia A. Answer: PTT
●● a patient presents with a PT of 17 seconds, PTT of 31, and TT of 16,
what factor deficiency is most likely. Answer: VII
●● what subtype of vWD gives a positive response. Answer: 2b
●● what molecule does unfractionated heparin bind to in precipitating
its anticoagulation. Answer: antithrombin
●● what efficacy would IVIG serve in treatment of ITP. Answer: keeps
IgG coated platelets in circulation
●● Which of the following is disorder of aggregation?. Answer:
glanzmanns thromboasthenia
●● A female patient, 45 yrs old, comes into the Emergency Room
complaining of bruises on their forearm and epistaxis. Lab results
PAPER 2026 FULL QUESTIONS AND
CORRECT ANSWERS GRADED A+
●● in this sex-linked recessive disorder, a common clinical finding is
hemarthrosis, normal platelet count, normal RIPA. Answer: hemophilia
A
●● In this type of vWD, pt count is normal, PTT is prolonged, vwF
antigen is very low or absent, RIPA is absent and all vWF multimers are
absent:. Answer: type 3
●● which of the following is recognized as viable treatment for TTP.
Answer: plasma exchange
●● all of the following may be seen in HUS. Answer: decreased
reticulocyte count
●● all of the following are associated with HELLP syndrome except:.
Answer: absence of schistocytes
●● In this rare recessive disorder, patients are missing the radius bone
and present with an elevated WBC count and decreased platelet count.
Answer: TAR syndrome
,●● In this syndrome platelets are lacking dense granules, and present
with oculocutaneous albinism, bleeding gums, and excessive bleeding
after surgery:. Answer: hermansky-pullak
●● which TEG parameter should let the clinical know a platelet
transfusion is indicated. Answer: decreased MA
●● in this autosomal disorder clot extraction is abnormal. Answer:
glanzmanns thromboasthenia
●● what is considered normal range for bleeding time. Answer: 2-9
minutes
●● which of the following disorders charactered by lack of alpha
granules. Answer: gray platelet
●● test measured for platelet plug to occlude the area. Answer: PFA-100
●● When running TEG, what reagent will be unemployed in the test
system for a pt on unfractionated heparin?. Answer: Heparinase
●● all of the following coagulation factor are measured in the
prothrombin complex time test except. Answer: Factor 13 (XIII)
,●● what does ISI stand for. Answer: international sensitivity index
●● all of the following are measured by the APTT except. Answer:
Factor 7 (VII)
●● This screening test for factor V involves adding a standard amount of
activated protein C for both patient plasma and normal plasma. Answer:
APTT
●● what test is elevated in uncompensated DIC. Answer: d-dimer
●● light transmittance is increased in platelet aggregation studies where
the platelet agonist employed is ADP. Answer: true
●● Patients who have deficiency in GP1B have a deficiency in adhesion.
Answer: true
●● oral anticoagulant. Answer: vitamin k
●● which of the following is decreased in uncompensated DIC. Answer:
fibrinogen
●● DDVAP is an effective treatment of. Answer: vWD type 1
, ●● what would mixing studies reveal in a patient with an inhibitor to
factor VIII. Answer: APPTT would not correct with absorbed plasma or
normal plasma
●● which of the following tests is increased in a patient with severe
hemophilia A. Answer: PTT
●● a patient presents with a PT of 17 seconds, PTT of 31, and TT of 16,
what factor deficiency is most likely. Answer: VII
●● what subtype of vWD gives a positive response. Answer: 2b
●● what molecule does unfractionated heparin bind to in precipitating
its anticoagulation. Answer: antithrombin
●● what efficacy would IVIG serve in treatment of ITP. Answer: keeps
IgG coated platelets in circulation
●● Which of the following is disorder of aggregation?. Answer:
glanzmanns thromboasthenia
●● A female patient, 45 yrs old, comes into the Emergency Room
complaining of bruises on their forearm and epistaxis. Lab results
