![]() |
مستوى رآبـع..hematology
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 |
رد: مستوى رآبـع..hematology
هذي نفسها الاسألة الي اخذتها من الدكتور الترم الي راااح لكن ابد ماجا منها الا من 7 لين 10 اسألة
ذاكروو الاسألة والكتاب اهم شي |
رد: مستوى رآبـع..hematology
|
رد: مستوى رآبـع..hematology
هلا بك خيو الله يستر يب اخذتها من الدكتورة قالت لي مهمه عاد متري قلت اساعد اللي يبيها يعطيك الف عافيه ربي يوفقك يارب |
رد: مستوى رآبـع..hematology
والله على اللي عندي...ان شاءالله استفيد منها.. بس السؤال اللي في بالي
تعتقدون انو فيه مقالي:mh12: وشاكره لكم تفاعلكم.. |
رد: مستوى رآبـع..hematology
هلا غلاتي مابتوقع سالنا الدكتوره قالت لو فيه كتابي كان جاهم قرار بس ماجاهم شي فديتك ربي يوفقكم |
All times are GMT +3. الوقت الآن حسب توقيت السعودية: 02:46 PM. |
Powered by vBulletin® Version 3.8.7, Copyright ©2000 - 2025, Jelsoft Enterprises Ltd. جامعة الملك
الفيصل,جامعة الدمام
المواضيع والمشاركات في الملتقى تمثل اصحابها.
يوجد في الملتقى تطوير وبرمجيات خاصة حقوقها خاصة بالملتقى
ملتزمون بحذف اي مادة فيها انتهاك للحقوق الفكرية بشرط مراسلتنا من مالك المادة او وكيل عنه