University : The Tamil Nadu Dr. MGR University
Course : D.M. – CLINICAL HAEMATOLOGY Degree Examination
Subject : Paper II – LABORATORY HAEMATOLOGY
Question Paper Code : 161402
Subject Code : 1402
Year of Exam : 2015
(LG 065) FEBRUARY 2015 Sub. Code:1402
D.M. – CLINICAL HAEMATOLOGY
Paper II – LABORATORY HAEMATOLOGY
Q.P.Code: 161402
Time: Three Hours Maximum: 100 Marks
I. Elaborate on: (2 x 15 = 30)
1. Discuss evolution of laboratory tests for HLA typing and discuss its relevance in allogeneic stem cell transplantation.
2. Describe the tests used for evaluation of megaloblastic anemia and discuss the advantages and disadvantages of each of them.
II. Write notes on: (10 x 7 = 70)
1. Sideroblasts.
2. Immature platelet fraction.
3. HbH diagnosis.
4. Diagnosis of CMV re-activation and disease.
5. Evaluation for inhibitors in patients with hemophilia.
6. Diagnosis of Glanzmans thrombasthenia.
7. Genetics of severe combined immune-deficiency
8. Diagnosis of chronic granulomatous disease
9. Antenatal diagnosis and thalassemia
10. Mixed field reaction on Blood Group typing
Course : D.M. – CLINICAL HAEMATOLOGY Degree Examination
Subject : Paper II – LABORATORY HAEMATOLOGY
Question Paper Code : 161402
Subject Code : 1402
Year of Exam : 2015
(LG 065) FEBRUARY 2015 Sub. Code:1402
D.M. – CLINICAL HAEMATOLOGY
Paper II – LABORATORY HAEMATOLOGY
Q.P.Code: 161402
Time: Three Hours Maximum: 100 Marks
I. Elaborate on: (2 x 15 = 30)
1. Discuss evolution of laboratory tests for HLA typing and discuss its relevance in allogeneic stem cell transplantation.
2. Describe the tests used for evaluation of megaloblastic anemia and discuss the advantages and disadvantages of each of them.
II. Write notes on: (10 x 7 = 70)
1. Sideroblasts.
2. Immature platelet fraction.
3. HbH diagnosis.
4. Diagnosis of CMV re-activation and disease.
5. Evaluation for inhibitors in patients with hemophilia.
6. Diagnosis of Glanzmans thrombasthenia.
7. Genetics of severe combined immune-deficiency
8. Diagnosis of chronic granulomatous disease
9. Antenatal diagnosis and thalassemia
10. Mixed field reaction on Blood Group typing
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