KL 2813
Second Year MBBS Examination
II MBBS Pathology Paper 1
Date: 07-06-2017 Time: 2 hours
Max
Instructions:
1. Answer to the points.
2. Figure to the right indicates marks.
3. Use separate answer books for each section.
5. Write legibly.
Section 1
1. MCQ (10)
a. Mutation affecting germ cells produce: (a) Cancers (B)Inherited diseases
b. Most common hereditary coagulation disorder is:(A)Hemophilia A
(B)Hemophilia B (C)von Willebrand disease (D)Protein C deficiency
c. Basophils are increased in: (A) Bronchial asthma (B)Chronic Myeloid
Leukemia (C)Pneumonia (D)Corticosteroid therapy
e. In cell cycle signal transduction system is activated by(a) G protein
receptors(b) Selectins(c) Cadherins(d) Integrins
f. In hereditary spherocytosis following membrane structure is deficient: (a)
Band 3 protein(B) Glycophorin(c) Spectrin(d) Glycolipid
Bax
h. In iron deficiency anemia TIBC is: (a) Low(b) High(c) Normal (d) Borderline
i. The most common form of amyloid in developing countries is:(a) Primary (b)
Secondary (c) Localised (d) Hereditary
2. Write short notes on: (two out of three) (10)
a. Describe intracellular accumulation. Write fatty change in detail.
b. Write about factors influencing tissue repair.
c. Disseminated intravascular coagulation.
a. Laboratory diagnosis of Chronic Myeloid Leukemia.
b. Hemolytic anaemia due to intracellular etiology.
c. Fresh frozen plasma.
d. Rh blood group system.
a. Paraneoplastic syndrome.
b. Granulomatous inflammation.
***
Second Year MBBS Examination
II MBBS Pathology Paper 1
Date: 07-06-2017 Time: 2 hours
Max
--- Content provided by FirstRanker.com ---
Marks: 40Instructions:
1. Answer to the points.
2. Figure to the right indicates marks.
3. Use separate answer books for each section.
--- Content provided by FirstRanker.com ---
4. Draw diagrams wherever necessary.5. Write legibly.
Section 1
1. MCQ (10)
a. Mutation affecting germ cells produce: (a) Cancers (B)Inherited diseases
--- Content provided by FirstRanker.com ---
(c)Congenital Malformations (D)Aneuploidyb. Most common hereditary coagulation disorder is:(A)Hemophilia A
(B)Hemophilia B (C)von Willebrand disease (D)Protein C deficiency
c. Basophils are increased in: (A) Bronchial asthma (B)Chronic Myeloid
Leukemia (C)Pneumonia (D)Corticosteroid therapy
--- Content provided by FirstRanker.com ---
d. (A)Edward Jenner (B) Hippocrates (C)Karl Landsteiner (D)Laennece. In cell cycle signal transduction system is activated by(a) G protein
receptors(b) Selectins(c) Cadherins(d) Integrins
f. In hereditary spherocytosis following membrane structure is deficient: (a)
Band 3 protein(B) Glycophorin(c) Spectrin(d) Glycolipid
--- Content provided by FirstRanker.com ---
g. Which of the following gene is proapoptotoic? (a) p53 (b) Bel-2 (c) RB (d)Bax
h. In iron deficiency anemia TIBC is: (a) Low(b) High(c) Normal (d) Borderline
i. The most common form of amyloid in developing countries is:(a) Primary (b)
Secondary (c) Localised (d) Hereditary
--- Content provided by FirstRanker.com ---
Section 22. Write short notes on: (two out of three) (10)
a. Describe intracellular accumulation. Write fatty change in detail.
b. Write about factors influencing tissue repair.
c. Disseminated intravascular coagulation.
--- Content provided by FirstRanker.com ---
3. Write briefly on: (four out of five) (10)a. Laboratory diagnosis of Chronic Myeloid Leukemia.
b. Hemolytic anaemia due to intracellular etiology.
c. Fresh frozen plasma.
d. Rh blood group system.
--- Content provided by FirstRanker.com ---
4. Write short notes on: (two out of three) (10)a. Paraneoplastic syndrome.
b. Granulomatous inflammation.
***