جـنـونـي غـير
2011- 6- 10, 09:15 PM
صباحكم / مساكم ورد
هذي اسئله اخذتها من الدكتورة نفسها للهمتولجي
اتمنى تنفعكم :
1 ) Poikilocytosis is:
a) Variation in red cell size.
b) Variation in red cell color.
c) Variation in red cell shape.=
d) None of the above.
red cell fragments?
a) Echinocyte.
b) Elliptocyte.
c) Schistocyte. =
d) Stomatocyte.
It is a defect of the red cell membrane( -
a) Thalassemia.
b) Sickle cell anemia.
c) Hereditary spherocytosis.=
d) Megaloblastic anemia.
4) All of the following is correct regarding spherocytosis…except:
a) Normocytic Normochromic anemia.
b) Decreased reticulocyte count.=
c) Raised plasma bilirubin.
d) Increased osmotic fragility.
5) Heinz bodies in the red cells are seen in cases of:
a) Hereditary sherocytosis.
b) Hereditary elliptocytosis.
c) Glucose-6-phosphate dehydrogenase deficiency.=
d) Sickle cell anemia.
6) ………………….is caused by substitution of one amino acid (valine) instead of glutamic acid at position no.6 in the beta chain of hemoglobin:
a) Hb-A.
b) Hb-A2.
c) Hb-F.
d) Hb-S.=
7) Atrophy of the spleen, is seen in cases of:
a) Thalassemia.
b) Sickle cell anemia.=
c) G6PD deficiency.
d) Hereditary elliptocytosis.
8) Iron deficiency lead to:
a) Normocytic Normochromic anemia.
b) Microcytic hypochromic anemia.=
c) Macrocytic anemia.
d) Hemolytic anemia.
9) Neurological symptoms are seen in cases of:
a) Iron deficiency anemia.
b) Folic acid deficiency.
c) Vitamin B12 deficiency.=
d) All of the above.
10) Schilling test is done to diagnose of:
a) Sickle cell anemia.
b) Thalassemia.
c) Pernicious anemia.=
d) Folic acid deficiency.
11)Megaloblastic hematopoiesis is seen in cases of :
a) Iron deficiency.
b) Folic acid deficiency.=
c) G6PD deficiency.
d) Vitamin C deficiency.
12) Fanconi's anemia is a type of:
a) Vitamin B12 deficiency.
b) Aplastic anemia.=
c) Thalassemia.
d) Folic acid deficiency anemia.
13) The most abundant leukocyte in a normal blood smear:
a) Lymphocytes.
b) Monocytes.
c) Eosinophils.
d) Neutrophils. =
14) The first line of defence against parasites:
a) Neutrophils.
b) Basophils.
c) Eosinophils.=
d) Lymphocytes.
15) ………………play a role in immediate and delayed hypersensetivity:
a) Monocytes.
b) Lymphocytes.
c) Eosinophils.
d) Basophils. =
16) The largest leukocyte is:
a) Neutrophil.
b) Lymphocyte.
c) Monocyte.=
d) Basophil.
17) Cell which participates in cell-mediated immunity:
a) Monocyte.
b) B-lymphocyte.
c) T-lymphocyte.=
d) Neutrophil.
18) …………….promotes blood clotting and help to prevent blood loss from damaged blood vessels:
a) Platelets.=
b) WBCs.
c) RBCs.
d) All of the above.
19) ………………converts fibrinogen to fibrin:
a) Prothrombin.
b) Thrombin.=
c) Plasminogen.
d) Plasmin.
20) Antibody-induced haemolytic disease in the new born that is caused by blood group incompatibility between mother and fetus:
a) Hemolytic ureamic syndrome.
b) Erythroblastosis fetalis.=
c) Hereditary spherocytosis.
d) Thrombotic thrombocytopenic purpura.
21) Ovalocytes are seen in cases of:
a) Iron deficiency anemia.=
b) Thalassemia.
c) Folate deficiency.
d) All of the above.
22) Red cell with central dark area:
a) Stomatocyte.
b) Spherocyte.
c) Target cell.=
d) Teardrop cell.
23) Young red cell with cytoplasmic RNA:
a) Spherocyte.
b) Reticulocyte.=
c) Stomatocyte.
d) Elliptocyte.
24) The specific haemoglobin binding protein in the plasma is:
a) Bilirubin.
b) Haptoglobin.=
c) Myoglobin.
d) None of the above.
25) Acute blood loss usually results in:
a) Microcytic hypochromic anemia.
b) Normocytic normochromic anemia.=
c) Macrocytic anemia.
d) None of the above.
26) Normal adult haemoglobin tetramer is:
a) 2 alpha: 2 gama. =
b) 2 alpha: 2 beta.
c) 2 alpha: 2 delta.
d) 2 beta : 2 gama.
27)…………………..represent 2 – 4 % of total leukocyte:
a) Neutrophils.
b) Basophils.
c) Eosinophils. =
d) Monocytes.
28) ………………..are small cytoplasmic fragments derived from megakaryocyte:
a) RBCs.
b) WBCs.
c) Platelets.=
d) None of the above.
29) A decrease in the number of platelets is:
a) Thrombocytopenia.=
b) Thrombocytosis.
c) Thrombosis.
d) Thrombopoiesis.
30) …………………is the reduction in the amount of circulating Hemoglobin,red blood cells or both:
a) Polycythemia.
b) Anemia.=
c) Hemophila.
d) Leukopenia.
اتمنى لكم التوفيق ،،
ادعولي بإختباري بكره فديتكم
لكم ودي
هذي اسئله اخذتها من الدكتورة نفسها للهمتولجي
اتمنى تنفعكم :
1 ) Poikilocytosis is:
a) Variation in red cell size.
b) Variation in red cell color.
c) Variation in red cell shape.=
d) None of the above.
red cell fragments?
a) Echinocyte.
b) Elliptocyte.
c) Schistocyte. =
d) Stomatocyte.
It is a defect of the red cell membrane( -
a) Thalassemia.
b) Sickle cell anemia.
c) Hereditary spherocytosis.=
d) Megaloblastic anemia.
4) All of the following is correct regarding spherocytosis…except:
a) Normocytic Normochromic anemia.
b) Decreased reticulocyte count.=
c) Raised plasma bilirubin.
d) Increased osmotic fragility.
5) Heinz bodies in the red cells are seen in cases of:
a) Hereditary sherocytosis.
b) Hereditary elliptocytosis.
c) Glucose-6-phosphate dehydrogenase deficiency.=
d) Sickle cell anemia.
6) ………………….is caused by substitution of one amino acid (valine) instead of glutamic acid at position no.6 in the beta chain of hemoglobin:
a) Hb-A.
b) Hb-A2.
c) Hb-F.
d) Hb-S.=
7) Atrophy of the spleen, is seen in cases of:
a) Thalassemia.
b) Sickle cell anemia.=
c) G6PD deficiency.
d) Hereditary elliptocytosis.
8) Iron deficiency lead to:
a) Normocytic Normochromic anemia.
b) Microcytic hypochromic anemia.=
c) Macrocytic anemia.
d) Hemolytic anemia.
9) Neurological symptoms are seen in cases of:
a) Iron deficiency anemia.
b) Folic acid deficiency.
c) Vitamin B12 deficiency.=
d) All of the above.
10) Schilling test is done to diagnose of:
a) Sickle cell anemia.
b) Thalassemia.
c) Pernicious anemia.=
d) Folic acid deficiency.
11)Megaloblastic hematopoiesis is seen in cases of :
a) Iron deficiency.
b) Folic acid deficiency.=
c) G6PD deficiency.
d) Vitamin C deficiency.
12) Fanconi's anemia is a type of:
a) Vitamin B12 deficiency.
b) Aplastic anemia.=
c) Thalassemia.
d) Folic acid deficiency anemia.
13) The most abundant leukocyte in a normal blood smear:
a) Lymphocytes.
b) Monocytes.
c) Eosinophils.
d) Neutrophils. =
14) The first line of defence against parasites:
a) Neutrophils.
b) Basophils.
c) Eosinophils.=
d) Lymphocytes.
15) ………………play a role in immediate and delayed hypersensetivity:
a) Monocytes.
b) Lymphocytes.
c) Eosinophils.
d) Basophils. =
16) The largest leukocyte is:
a) Neutrophil.
b) Lymphocyte.
c) Monocyte.=
d) Basophil.
17) Cell which participates in cell-mediated immunity:
a) Monocyte.
b) B-lymphocyte.
c) T-lymphocyte.=
d) Neutrophil.
18) …………….promotes blood clotting and help to prevent blood loss from damaged blood vessels:
a) Platelets.=
b) WBCs.
c) RBCs.
d) All of the above.
19) ………………converts fibrinogen to fibrin:
a) Prothrombin.
b) Thrombin.=
c) Plasminogen.
d) Plasmin.
20) Antibody-induced haemolytic disease in the new born that is caused by blood group incompatibility between mother and fetus:
a) Hemolytic ureamic syndrome.
b) Erythroblastosis fetalis.=
c) Hereditary spherocytosis.
d) Thrombotic thrombocytopenic purpura.
21) Ovalocytes are seen in cases of:
a) Iron deficiency anemia.=
b) Thalassemia.
c) Folate deficiency.
d) All of the above.
22) Red cell with central dark area:
a) Stomatocyte.
b) Spherocyte.
c) Target cell.=
d) Teardrop cell.
23) Young red cell with cytoplasmic RNA:
a) Spherocyte.
b) Reticulocyte.=
c) Stomatocyte.
d) Elliptocyte.
24) The specific haemoglobin binding protein in the plasma is:
a) Bilirubin.
b) Haptoglobin.=
c) Myoglobin.
d) None of the above.
25) Acute blood loss usually results in:
a) Microcytic hypochromic anemia.
b) Normocytic normochromic anemia.=
c) Macrocytic anemia.
d) None of the above.
26) Normal adult haemoglobin tetramer is:
a) 2 alpha: 2 gama. =
b) 2 alpha: 2 beta.
c) 2 alpha: 2 delta.
d) 2 beta : 2 gama.
27)…………………..represent 2 – 4 % of total leukocyte:
a) Neutrophils.
b) Basophils.
c) Eosinophils. =
d) Monocytes.
28) ………………..are small cytoplasmic fragments derived from megakaryocyte:
a) RBCs.
b) WBCs.
c) Platelets.=
d) None of the above.
29) A decrease in the number of platelets is:
a) Thrombocytopenia.=
b) Thrombocytosis.
c) Thrombosis.
d) Thrombopoiesis.
30) …………………is the reduction in the amount of circulating Hemoglobin,red blood cells or both:
a) Polycythemia.
b) Anemia.=
c) Hemophila.
d) Leukopenia.
اتمنى لكم التوفيق ،،
ادعولي بإختباري بكره فديتكم
لكم ودي