Multiple Choice
__________ is a rare autosomal recessive disorder of platelet function associated with an abnormality of membrane glycoproteins IIb and IIIa, causing decreased platelet aggregation.
A) Bernard-Soulier syndrome
B) Glanzmann's thrombasthenia
C) von Willebrand's disease
D) Congenital afibrinogenemia
E) None of the above
Correct Answer:

Verified
Correct Answer:
Verified
Q5: von Willebrand's disease (vWD) and Bernard-Soulier syndrome
Q6: The most important therapeutic intervention for suspected
Q7: _ is a common clinical manifestation of
Q8: The malignant paraproteins result in:<br>A) Coagulation abnormalities<br>B)
Q9: Individuals with chronic liver disease are often
Q11: Thrombocytosis is classified as:<br>A) Platelet count <400
Q12: All of the following factors are decreased
Q13: The P1<sup>A1 </sup>antigen is found in _
Q14: All of the following disorders have been
Q15: Uremia is a _ platelet disorder.<br>A) Congenital<br>B)