What is the amino acid substitution in patients with sickle cell anemia?
Thalassemia and Hemoglobinopathy

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University
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Medium

Sheryl Schloss
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20 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
adenine for thymine
lysine for valine
valine for glutamic acid
glutamic acid for valine
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following factors contributes to the pathophysiology of sickling?
increased iron concentration
hypochromia
fava beans
dehydration
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following shows crystals like those seen here
Hgb CC disease
Hgb DD disease
Hgb EE disease
Hgb SC disease
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
The crystals seen here are associated with:
Hgb CC disease
Hgb SS disease
Hgb SC disease
Hgb EE disease
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
All but one of the following may be seen in the PB smear when a sickle cell crisis has occurred
Target cells
NRBCs
Polychromasia
Moderate elliptocytes
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
List two sets of lab data that can distinguish IDA from beta thalassemia trait.
Serum iron and RBC
Hgb and Hct
WBC and RDW
RBC indices and Platelets
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the majority hemoglobin in beta thalassemia major
Hgb A
Hgb A2
Hgb F
Hgb H
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