1-Commonest cause of Budd Chiari syndrome is
2-The Immunoglobulin least commonly involved in Multiple Myeloma is
3-Most common inherited bleeding disorder is-
4-Best marker for Iron deficiency is
5-All of the following are the good prognostic features of Hodgkin’s disease except-
6-Sickle cell anemia leads to resistance towards
7-The most important diagnostic feature for Beta thalassaemiatrait-
8-RDW is an indication of which of the following-
9-The following Protein defects can causes hereditiary spherocytosis except
10- A 10 day old male is being seen in the emergency room due lethargy and poor feeding. Her anterior fontanel is full. A CT scan demonstrates an intraparenchymal hemorrhage. Coagulation tests are ordered with the following results: PT—37 seconds (normal 9.7-11.2 seconds) and a PTT of 66 seconds (normal 22-36 seconds). This child may have which of the following factor deficiencies:
11- A 5 year old male presents with fulminant acute hepatic failure. He is noted to be bleeding from his gums, nose and has hematochezia. This patient’s bleeding is most likely due to which of the following combinations:
12-Shilling’s test is used to determine the deficiency of
13- The blood disease which is caused by the occurrence of mutations in hemoglobin genes is
14- All the following are example of diseases causing aplastic anemia except-
15-False statement regarding DIC is-
16-Palpable purpura is seen in
17-Thrombocytopenia is not seen in-
18-Crew haircut appearance in Xray skull and Gandy gamma bodies are seen in-
19- A 2-year-old girl presents with prolonged oozing from her tongue after apparently biting it. Her platelet count is normal. Her PT is 68 seconds (normal range is 9–12 seconds), her aPTT is 123 seconds (normal range is 22–33 seconds) and her thrombin time is 58 seconds (normal range is 12–18 seconds). Which of the following tests should be ordered next?
20-Ring sideroblast are characteristically seen in-
21-Massive splenomegaly is least likely to be associated with wich of the following-
22- Iron absorption is increased in all except-
23-Hair on appearance is seen in X-rays skull in-
24-Coombs positive hemolytic anemia associated with-
25-Pawn ball megakaryocytes are characteristics of-
26- A 6 year old girl preset with repeated episodes od bleeding into joints. APTT is prolonged and PT is normal. The most likely diagnosis is-
27-Which of the following is not involved in intrinsic pathways-
28-Deficiency of intrinsic factor of castle causes-
29-Reticulocytosis is NOT a feature of-
30-Raised serum alkaline phosphatase is seen in all except
31-Russell body found in-
32-Commenest site of lytic lesion in case of multiple myeloma is
33-The most common type of ALL is-
34-Secondary Polycythemia may seen in-
35-Gaisbock syndrome is known as-
36-Which of the following is caused by deletion of all four alpha globin genes-
37-Anemia due to antibodies against blood group antigens-
38-PNH is associated with all of the following condition except-
39-Lab. Evaluation for the differential diagnosis of Chronic myeloproliferative disorders include all of the following except
40-In Burkitts lymphoma , translocation seen in chromosome-
41-Best prognostic type of Hodgkin’s lymphoma is-
42- All are true for sickle cell anemia ,except-
43-Hypercoagulability due to defective factor V gene is called-
44-Diagnostic of beta thalassemia is established by
45-Mentzer index more than 13 suggest a diagnosis of-
47-Maximum ESR is seen in-
48-Most common heavy chain disease is-
49-The marker for B lymphocyte is-
50-In Ritcher’s transformation CLLtransform into-
