UAMS_HEME_LAB_PRACTICAL_3_COMPREHENSIVE_EXAM_2026_QUESTIONS_AND.pdf

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Institution LAB PRACTICAL

Course LAB PRACTICAL

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UAMS_HEME_LAB_PRACTICAL_3_COMPREHENSIVE_EXAM_2026_QUESTIONS_AND.pdf

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UAMS HEME LAB PRACTICAL 3
COMPREHENSIVE EXAM
QUESTIONS AND ANSWERS
GRADED A PLUS
◉ if VIII:vWF is deficient. Answer: Von Willebrand Disease
Factor VIII:C is also deficient, prolonged PTT

◉ What does VIII:vWF do. Answer: attaches collagen to glycoprotein
IB on platelet surface

◉ Difference between Hemophilia A and vWD. Answer: Hemophilia
A has normal bleeding time, Rist agg, vWFR:Co, and vWF:Ag

vWD is abnormal for all

◉ how is Hemophilia A inherited. Answer: recessive, X-linked

◉ How is vWD inherited. Answer: dominant, autosomal

◉ Platelet agg studies measure. Answer: primary and secondary
aggregation with various aggregates such as ADP

, ◉ What does an abnormal aggregation graph indicate. Answer:
platelet membrane defect
aspirin use
storage pool defect

◉ What agonist with an abnormal aggregation indicates vWD.
Answer: ristocetin

◉ Bernard Soulier disease. Answer: GPIb/IX/V complex is missing
on plt surface

◉ abnormal plt agg with bernard soulier disease. Answer: ristocetin
ristocetin and vWF

◉ Glanzmanns thrombasthenia. Answer: Defective plt membrane GP
IIb/IIIa

◉ abnormal plt agg with Glanzmanns. Answer: unable to find
fibrinogen
ADP
Collagen
Epinephrine

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Uploaded on: August 19, 2026
Number of pages: 12
Written in: 2026/2027
Type: Exam (elaborations)
Contains: Questions & answers

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