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CPTC: HEMATOLOGY: CHAPTER 8: THE NORMOCHROMIC ANEMIAS CAUSED BY HEMOGLOBINOPATHIES EXAM QUESTIONS AND ANSWERS VERIFIED 100% GUARANTEED PASS $9.99
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CPTC: HEMATOLOGY: CHAPTER 8: THE NORMOCHROMIC ANEMIAS CAUSED BY HEMOGLOBINOPATHIES EXAM QUESTIONS AND ANSWERS VERIFIED 100% GUARANTEED PASS
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CPTC: HEMATOLOGY: CHAPTER 8: THE NORMOCHROMIC ANEMIAS CAUSED BY HEMOGLOBINOPATHIES EXAM QUESTIONS AND ANSWERS VERIFIED 100% GUARANTEED PASS The hemoglobin variant that is seen frequently in the Southeast Asian population, and migrates with Hgb C at pH 8.6, is: A. Barts B. F C. E D. H C A b...

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  • October 29, 2024
  • 18
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers

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  • cptc hematology chapter 8 the normochromic anem

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CPTC: HEMATOLOGY: CHAPTER 8: THE NORMOCHROMIC

ANEMIAS CAUSED BY HEMOGLOBINOPATHIES EXAM

QUESTIONS AND ANSWERS VERIFIED 100% GUARANTEED

PASS


The hemoglobin variant that is seen frequently in the Southeast Asian population,

and migrates with Hgb C at pH 8.6, is:

A. Barts

B. F

C. E

D. H

C

A blood smear from a patient with sickle cell crisis shows 80 nucleated red cells

per 100 leukocytes. The total leukocyte count is 18 ´ 109/L. The corrected white

cell count is:

A. 17,200

B. 9,000

C. 10,000

D. 13,400

C

,A patient with sickle cell anemia may develop cardiopulmonary disease due to:

A. Untreated leg ulcers

B. High blood viscosity

C. Increased Hgb F levels

D. Hemolytic crisis

B

Autosplenectomy is characteristic of:

A. Sickle cell trait

B.Hgb C disease

C. Thalassemia

D. Sickle cell anemia

D

The Benin haplotype of sickle cell disease is prevalent in which country or

countries?

A. Saudi Arabia and Asia

B. Senegal

C. West Africa

D. Central and South Africa

C

When the bone marrow temporarily ceases to produce cells in a sickle cell

patient, a(n) _________ crisis has occurred.

A) aplastic

B) hemolytic

, C) vaso-occlusive

D) cardiac

A

Mr. Bennett was admitted with a hematocrit of 28%. He has a history of chronic

anemia, moderate splenomegaly, and recent retinal hemorrhages. His peripheral

smear reveals target cells, and some show structures jutting from the red cell

membrane. The most probable diagnosis is:

A)Hgb S-S

B)Hgb A-C

C)Hgb S-C

D)Hgb A-A

C

Sickle cell disease is best differentiated from sickle cell trait by:

A) Wright smear examination

B) Determination of fetal hemoglobin

C) Genetic testing

D) Hemoglobin electrophoresis

D

Which of the following "poikilocytes" are classically associated with

hemoglobinopathies and liver disease?

A)Spherocytes

B)Sickle cells

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