Von Willebrand Disease | Pathophysiology, Types, Symptoms and Treatment

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Health Sciences, Biology
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University - Vocational training
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Hard
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the primary cause of von Willebrand disease?
Deficiency of Factor X
Deficiency of von Willebrand factor
Deficiency of Factor IX
Excessive platelet production
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which chromosome is the von Willebrand factor gene located on?
Chromosome 12
Chromosome 21
Chromosome 7
Chromosome 18
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is one of the key roles of von Willebrand factor in hemostasis?
Inhibiting platelet aggregation
Increasing red blood cell production
Promoting platelet aggregation and adhesion
Reducing blood viscosity
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following is a common clinical feature of von Willebrand disease?
High blood pressure
Severe joint bleeding
Mucocutaneous bleeding
Excessive clotting
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What distinguishes Type 3 von Willebrand disease from other types?
It is inherited in an autosomal dominant manner
It only affects males
It involves a total absence of von Willebrand factor
It is the most common type
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which subtype of Type 2 von Willebrand disease is characterized by hyperfunctional platelet binding?
Type 2M
Type 2N
Type 2B
Type 2A
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a common diagnostic test for von Willebrand disease?
Kidney function test
Liver function test
Complete blood count (CBC)
Electrocardiogram (ECG)
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