Thalassemia and Hemoglobinopathy

Thalassemia and Hemoglobinopathy

University

20 Qs

quiz-placeholder

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Thalassemia and Hemoglobinopathy

Thalassemia and Hemoglobinopathy

Assessment

Quiz

Other

University

Medium

Created by

Sheryl Schloss

Used 39+ times

FREE Resource

20 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

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

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

Media Image

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

Media Image

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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