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HEMATOLOGY MCQ – Exercise 12

By | Published: September 25, 2015

The multiple choice questions in this online test paper focuses on HEMATOLOGY MCQ. If you are looking for self evaluation of your PG Medical entrance exam preparation then this online HEMATOLOGY MCQ Test Paper will help you to evaluate your exam preparation.

Instruction for REPRODUCTIVE BIOLOGY/ REPRODUCTIVE MEDICINE / INFERTILITY MCQs:

1- This online MCQ practice test paper contains 30 questions.
2- Each question in this online practice test paper have four options and only 1 option is correct.
3- You can view the answers of this practice test paper after submitting the practice test paper.
Note: The answers mentioned at the end of practice test are the best suitable option as per our knowledge. Users shall cross-check the answers with their textbooks.

Q 1. all are oral chelating agent except

 
 
 
 

Q 2. patients with β thalassemia trait have an elevated level of HbA2 of

 
 
 
 

Q 3. thalassemia features include all except

 
 
 
 

Q 4. Cooley’s anemia refers to

 
 
 
 

Q 5. parameter in fetal ultrasound is used to assess risk of hemoglobin Barts hydrops fetalis

 
 
 
 

Q 6. element found at the center of corrin ring in cobalamin is

 
 
 
 

Q 7. target cells can be seen in peripheral blood smear in which condition

 
 
 
 

Q 8. features of thalassemia includes all except

 
 
 
 

Q 9. following is normal or increased in thalassemia

 
 
 
 

Q 10. geographic distribution of the following closely resembles that of malaria

 
 
 
 

Q 11. thalassemic hemoglobinopathy includes

 
 
 
 

Q 12. patients who receive how many units of packed RBC develop hemosiderosis

 
 
 
 

Q 13. following α thalassemia resembles β thalassemia minor

 
 
 
 

Q 14. false regarding cobalamin

 
 
 
 

Q 15. in HbH disease how many of the 4 α globin loci are deleted

 
 
 
 

Q 16. presence of a palpable spleen in sickle cell disease ,suggests coexisting thalassemia

 
 
 
 

Q 17. following causes microcytic erythrocytosis

 
 
 
 

Q 18. methylcobalamin is the cofactor for

 
 
 
 

Q 19. body stores of cobalamin can suffice for how many years after supplies are completely cut off

 
 
 
 

Q 20. Hb Barts designated as

 
 
 
 

Q 21. deficiency of cobalamin is almost always due to

 
 
 
 

Q 22. Heinz bodies are

 
 
 
 

Q 23. estimated 5 year survival rate following allogeniic bone marrow transplantation

 
 
 
 

Q 24. following promotes high levels of HbF synthesis

 
 
 
 

Q 25. normal active physiologic mechanism of cobalamin absorption occurs in

 
 
 
 

Q 26. Lucarelli classification is used to classify

 
 
 
 

Q 27. in iron excess state which should be avoided

 
 
 
 

Q 28. form of cobalamin present in human plasma and in cell cytoplasm

 
 
 
 

Q 29. features of thalassemia includes all except

 
 
 
 

Q 30. variant hemoglobin that may be co-inherited with β thalassemia are

 
 
 
 


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