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Question 1
Incorrect
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Select one true statement about haemoglobin synthesis…
Your Answer: Produces the tetramer α2ß2 as the end result.
Correct Answer: Occurs in the cytosol of developing red cells.
Explanation:Haemoglobin (Hb) is synthesized in a complex series of steps. The haem part is synthesized in a series of steps in the mitochondria and the cytosol of immature red blood cells, while the globin protein parts are synthesized by ribosomes in the cytosol. Production of Hb continues in the cell throughout its early development from the proerythroblast to the reticulocyte in the bone marrow.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 2
Incorrect
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Choose the most correct answer, what reduces affinity for oxygen in haemoglobin?
Your Answer: Co2 in blood
Correct Answer: All the options are true
Explanation:The strength with which oxygen binds to haemoglobin is affected by several factors. These factors shift or reshape the oxyhaemoglobin dissociation curve. A rightward shift indicates that the haemoglobin under study has a decreased affinity for oxygen. The causes of shift to right can be remembered using the mnemonic, CADET, face Right! for CO2 and CO, Acid (H+), 2,3-DPG, Exercise and Temperature.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 3
Incorrect
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The actions of thrombin result directly in the release of:
Your Answer: Fibrin polymers
Correct Answer: Fibrin monomers
Explanation:Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalysing many other coagulation-related reactions.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 4
Incorrect
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Which statement is correct about the clinical state of methemoglobinemia?
Your Answer: Methaemoglobin, present in the circulation in small quantities, can resemble cyanosis.
Correct Answer: May arise due to a hereditary deficiency of NADH.
Explanation:Methaemoglobin is a form of haemoglobin that contains ferric [Fe3+] iron and has a decreased ability to bind oxygen. Spontaneously formed methaemoglobin is normally reduced by protective enzyme systems, e.g., NADH methaemoglobin reductase, hence a deficiency of NADH may result in increased levels of methaemoglobin
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This question is part of the following fields:
- Haematology
- Medicine
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Question 5
Correct
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Question 6
Incorrect
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What is the main function of vitamin E?
Your Answer: It is a cofactor in carbohydrate metabolism
Correct Answer: It is an antioxidant
Explanation:Vitamin E has many biological functions, the antioxidant function being the best known. Other functions include enzymatic activities, gene expression, and neurological function(s).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 7
Incorrect
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Which of the following foods contain Vitamin B 12?
Your Answer: Tomatoes
Correct Answer: Liver, meat
Explanation:No fungi, plants, nor animals (including humans) are capable of producing vitamin B12. Only bacteria and archaea have the enzymes needed for its synthesis. Proved food sources of B12 are animal products (meat, fish, dairy products).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 8
Incorrect
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Inactive cellular marrow is called
Your Answer: Red marrow
Correct Answer: Yellow marrow
Explanation:The two types of bone marrow are red marrow, which consists mainly of hematopoietic tissue, and yellow marrow, which is mainly made up of fat cells.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 9
Incorrect
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Which statement about antithrombin III is true?
Your Answer: It inactivates factors V and VIII
Correct Answer: It inhibits particularly factor II and X
Explanation:Antithrombin inactivates its physiological target enzymes, Thrombin (Factor II), Factor Xa and Factor IXa. ATIII binds to thrombin and then forms the thrombin-anti thrombin complex or TAT complex. This is a major natural pathway of anticoagulation. This binding of thrombin to AT is greatly enhanced in the presence of heparin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 10
Incorrect
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Which of the following foods do NOT contain high levels of folate?
Your Answer: Avocado
Correct Answer: Yellow vegetables
Explanation:Folate naturally occurs in a wide variety of foods, including vegetables (particularly dark green leafy vegetables), fruits and fruit juices, nuts, beans, peas, dairy products, poultry and meat, eggs, seafood, grains, and some beers. Avocado, beetroot, spinach, liver, yeast, asparagus, and Brussels sprouts are among the foods with the highest levels of folate
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This question is part of the following fields:
- Haematology
- Medicine
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Question 11
Correct
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In the normal adult, haematopoiesis is present
Your Answer: Axial skeleton and proximal ends of long bones
Explanation:In children, haematopoiesis occurs in the marrow of the long bones such as the femur and tibia. In adults, it occurs mainly in the pelvis, cranium, vertebrae, and sternum.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 12
Incorrect
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Synthesis of haem for haemoglobin occurs in the?
Your Answer: Nucleus of the white blood cells
Correct Answer: Mitochondria of the red blood cells
Explanation:Haemoglobin (Hb) is synthesized in a complex series of steps. The haem part is synthesized in a series of steps in the mitochondria and the cytosol of immature red blood cells, while the globin protein parts are synthesized by ribosomes in the cytosol.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 13
Incorrect
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The haemostatic plug formation in response to injured blood vessel wall is stimulated by exposure of which substance to platelets?
Your Answer: Tissue thromboplastin
Correct Answer: Collagen
Explanation:When the endothelium is damaged, the normally isolated, underlying collagen is exposed to circulating platelets, which bind directly to collagen with collagen-specific glycoprotein Ia/IIa surface receptors. This adhesion is strengthened further by von Willebrand factor (vWF), which is released from the endothelium and from platelets.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 14
Incorrect
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Where is Vitamin B 12 absorbed?
Your Answer: Liver
Correct Answer: Terminal ileum
Explanation:Protein-bound vitamin B12 must be released from the proteins by the action of digestive proteases in both the stomach and small intestine. Gastric acid releases the vitamin from food particles; therefore antacid and acid-blocking medications (especially proton-pump inhibitors) may inhibit absorption of B12. B12 must be attached to Intrinsic Factor (IF) for it to be efficiently absorbed, as receptors on the enterocytes in the terminal ileum of the small bowel only recognize the B12-IF complex; in addition, intrinsic factor protects the vitamin from catabolism by intestinal bacteria.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 15
Incorrect
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von Willebrand factor stabilises which clotting factor?
Your Answer: Factor V
Correct Answer: Factor VIII
Explanation:Von Willebrand factor’s primary function is binding to other proteins, in particular factor VIII, and it is important in platelet adhesion to wound sites. It is not an enzyme and, thus, has no catalytic activity. Factor VIII degrades rapidly when not bound to vWF. Factor VIII is released from vWF by the action of thrombin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 16
Incorrect
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Which of the following is matched correctly with regard to stem cells of the bone marrow?
Your Answer: None of the above
Correct Answer: Hemopoietic stem cells - basophils
Explanation:Hematopoietic stem cells (HSCs) or hemocytoblasts are the stem cells that give rise to all the other blood cells through the process of haematopoiesis. They give rise to both the myeloid and lymphoid lineages of blood cells. (Myeloid cells include monocytes, macrophages, neutrophils, basophils, eosinophils, erythrocytes, dendritic cells, and megakaryocytes or platelets. Lymphoid cells include T cells, B cells, and natural killer cells.)
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This question is part of the following fields:
- Haematology
- Medicine
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Question 17
Correct
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With regard to the spleen which of the following has the correct match?
Your Answer: Periarteriolar lymphoid sheets - T lymphocytes
Explanation:The spleen consists of:Red pulp – responsible for mechanical filtration of red blood cells. Red pulp contains sinusoids, which are filled with blood, splenic cords of reticular fibers and a marginal zoneWhite pulp – responsible for active immune response through humoral and cell-mediated pathways. Composed of nodules, called Malpighian corpuscles. These are composed of: lymphoid follicles, rich in B-lymphocytes and periarteriolar lymphoid sheaths, rich in T-lymphocytes
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This question is part of the following fields:
- Haematology
- Medicine
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Question 18
Correct
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Which of the following is a granulocyte?
Your Answer: Eosinophil
Explanation:Granulocytes are a category of white blood cells characterized by the presence of granules in their cytoplasm. There are three principal types of granulocytes, distinguished by their appearance under Wright’s stain:
- Basophil granulocytes
- Eosinophil granulocytes
- Neutrophil granulocytes
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This question is part of the following fields:
- Haematology
- Medicine
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Question 19
Correct
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Question 20
Incorrect
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Which of the following conditions is procoagulant?
Your Answer:
Correct Answer: Factor V Leiden
Explanation:Factor V Leiden is a genetic mutation of one of the clotting factors in the blood, Factor V. This mutation makes Factor V resistant to inactivation by activated Protein C, which normally helps to regulate clot formation. As a result, individuals with Factor V Leiden are at increased risk of developing abnormal blood clots (thrombophilia), making it a procoagulant condition.
The other conditions listed are associated with bleeding tendencies rather than increased clotting:
- Afibrinogenemia: A rare genetic disorder where there is a complete lack of fibrinogen, leading to bleeding problems.
- Hemophilia: A group of inherited bleeding disorders where blood does not clot properly due to the lack of sufficient blood-clotting proteins (factors VIII or IX).
- Hypothrombinemia: A condition characterized by low levels of prothrombin, leading to increased bleeding.
- Christmas disease (Hemophilia B): A form of hemophilia caused by a deficiency of factor IX, resulting in a bleeding tendency.
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This question is part of the following fields:
- Haematology
- Medicine
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