MMSC 423 HEMATOLOGY CERTIFICATION
TEST PAPER 2026 COMPLETE QUESTIONS
AND SOLUTIONS GRADED A+
●● Afibrigenemia. Answer: A prolonged PT, prolonged ATTP, prolonged
TT, undetectable fibrinogen by the Clauss method would be seen in:
a. Afibrigenemia
b. Hemophilia A
c. Hyperfibrinogenemia
d. Hypofibrinogenemia
●● hemophilia A. Answer: In this sex-linked recessive disorder, a
common clinical finding is hemathroses, normal platelet count, normal
RIPA, normal PT, prolonged APTT, and normal bleeding time
a. DIC
b. Factor X deficiency
c. Hemophilia A
d. ITP
●● type 3. Answer: in this type of vWD, the platelet count is normal,
PTT is prolonged, cWF antigen (vWFAg) is very low or absent. RIPA is
absent. And all vWF multimers are absent.
a. Type 1
,b. Type 2a
c. Type 2b
d. Type 3
●● plasma exchange. Answer: Which of the following is recognized as
viable treatment for TTP (thrombotic thrombocytopenic Purpura)?
a. All answers are correct
b. Cryoprecipiate
c. Plasma exchange
d. Platelet transfusion
●● decreased reticulocyte count. Answer: All of the following may be
seen in Hemolytic Uremic Syndrome, except:
a. Decreased reticulocyte count
b. Hematuria
c. Increased serum creatinine
d. Proteinuria
●● absence of shictocytes. Answer: All of the following are associated
with HELLP syndrome, except:
a. Absence of schistocytes
b. Anemia
c. Increased lactate dehydrogenase
, d. Proteinuria
●● TAR syndrome. Answer: In this rare autosomal recessive disorder,
patients are missing the radius bone and present with an elevated white
blood cell count and decreased platelet count
a. Bernard-Soulier
b. Gray platelet syndrome
c. Hermansky-pudlak syndrome
d. TAR syndrome
●● Hermansky Pudlak syndrome. Answer: In this syndrome, patients
platelets are lacking dense granules and present with oculocutaneous
albinism with bleeding diathesis often resulting in bleeding gums and
epistaxis as well as excessive bleeding following surgery.
a. Bernard-soulier syndrome
b. Glanzmann's thrombasthenia
c. Gray platelet syndrome
d. Hermansky-pudlak syndrome
●● decreased MA. Answer: Which TEG (thromboelastography)
parameter would let the clinician know a platelet transfusion is
indicated?
a. Decreased K time
b. Decreased MA
TEST PAPER 2026 COMPLETE QUESTIONS
AND SOLUTIONS GRADED A+
●● Afibrigenemia. Answer: A prolonged PT, prolonged ATTP, prolonged
TT, undetectable fibrinogen by the Clauss method would be seen in:
a. Afibrigenemia
b. Hemophilia A
c. Hyperfibrinogenemia
d. Hypofibrinogenemia
●● hemophilia A. Answer: In this sex-linked recessive disorder, a
common clinical finding is hemathroses, normal platelet count, normal
RIPA, normal PT, prolonged APTT, and normal bleeding time
a. DIC
b. Factor X deficiency
c. Hemophilia A
d. ITP
●● type 3. Answer: in this type of vWD, the platelet count is normal,
PTT is prolonged, cWF antigen (vWFAg) is very low or absent. RIPA is
absent. And all vWF multimers are absent.
a. Type 1
,b. Type 2a
c. Type 2b
d. Type 3
●● plasma exchange. Answer: Which of the following is recognized as
viable treatment for TTP (thrombotic thrombocytopenic Purpura)?
a. All answers are correct
b. Cryoprecipiate
c. Plasma exchange
d. Platelet transfusion
●● decreased reticulocyte count. Answer: All of the following may be
seen in Hemolytic Uremic Syndrome, except:
a. Decreased reticulocyte count
b. Hematuria
c. Increased serum creatinine
d. Proteinuria
●● absence of shictocytes. Answer: All of the following are associated
with HELLP syndrome, except:
a. Absence of schistocytes
b. Anemia
c. Increased lactate dehydrogenase
, d. Proteinuria
●● TAR syndrome. Answer: In this rare autosomal recessive disorder,
patients are missing the radius bone and present with an elevated white
blood cell count and decreased platelet count
a. Bernard-Soulier
b. Gray platelet syndrome
c. Hermansky-pudlak syndrome
d. TAR syndrome
●● Hermansky Pudlak syndrome. Answer: In this syndrome, patients
platelets are lacking dense granules and present with oculocutaneous
albinism with bleeding diathesis often resulting in bleeding gums and
epistaxis as well as excessive bleeding following surgery.
a. Bernard-soulier syndrome
b. Glanzmann's thrombasthenia
c. Gray platelet syndrome
d. Hermansky-pudlak syndrome
●● decreased MA. Answer: Which TEG (thromboelastography)
parameter would let the clinician know a platelet transfusion is
indicated?
a. Decreased K time
b. Decreased MA
