MMSC 423 HEMATOLOGY EXAMPREP
STUDY GUIDE 2026 DETAILED 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)
STUDY GUIDE 2026 DETAILED 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)
