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Question 1
Correct
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The extrinsic coagulation pathway is initiated by activation of which clotting factor?
Your Answer: Factor VII
Explanation:The tissue factor pathway (extrinsic) begins following damage to the blood vessel. FVII leaves the circulation and comes into contact with tissue factor (TF) expressed on tissue-factor-bearing cells (stromal fibroblasts and leukocytes), forming an activated complex (TF-FVIIa).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 2
Correct
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The following occurs as a result of 2,3 Bisphosphoglycerate binding to deoxyhaemoglobin
Your Answer: A reduction in deoxyhaemoglobin's affinity for oxygen
Explanation:2,3-BPG acts as a heteroallosteric effector of haemoglobin, lowering haemoglobin’s affinity for oxygen by binding preferentially to deoxyhaemoglobin. An increased concentration of BPG in red blood cells favours formation of the T, low-affinity state of haemoglobin and so the oxygen-binding curve will shift to the right.
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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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Which of the following is a granulocyte?
Your Answer: Monocyte
Correct 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 4
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 5
Incorrect
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Which vitamin plays a major role in the metabolism of many amino acids?
Your Answer: Vitamin B12
Correct Answer: Vitamin B6
Explanation:Vitamin B6 is part of the vitamin B group, and its active form, pyridoxal 5′-phosphate (PLP) serves as a coenzyme in many enzyme reactions in amino acid, glucose, and lipid metabolism.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 6
Correct
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What is the average life span of red blood cells?
Your Answer: 4 months
Explanation:Approximately 2.4 million new erythrocytes are produced per second in human adults. The cells develop in the bone marrow and circulate for about 100–120 days (4 months) in the body before their components are recycled by macrophages.
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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 these vitamins is not found in plants?
Your Answer: Folate
Correct Answer: Vitamin B12
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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Which of the following foods do NOT contain high levels of folate?
Your Answer: Eggs
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 9
Incorrect
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Which clotting factor is responsible for stabilization of the fibrin clot by formation of covalent cross-linkages?
Your Answer: Factor II
Correct Answer: Factor XIIIa
Explanation:Factor XIII or fibrin stabilizing factor is an enzyme of the blood coagulation system that crosslinks fibrin. Deficiency of this factor (FXIIID) affects clot stability.
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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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Choose the correct statement regarding the protein C/S system?
Your Answer: The system ultimately decreases the formation of plasmin.
Correct Answer: The protein C/S complex inactivates factor Va and VIIIa
Explanation:The best characterized function of Protein S is its role in the anti coagulation pathway, where it functions as a cofactor to Protein C in the inactivation of Factors Va and VIIIa.
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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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Where is the most erythropoietin produced?
Your Answer: Kidneys
Explanation:Erythropoietin is produced by interstitial fibroblasts in the kidney in close association with peritubular capillary and proximal convoluted tubule. It is also produced in perisinusoidal cells in the liver. While liver production predominates in the fetal and perinatal period, renal production is predominant during adulthood.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 12
Correct
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Which of the following cells will degranulate and release histamine when binding to IgE?
Your Answer: Basophils
Explanation:Basophils have protein receptors on their cell surface that bind IgE, an immunoglobulin involved in microparasite defence and allergy. When activated, basophils degranulate to release histamine, proteoglycans (e.g. heparin and chondroitin), and proteolytic enzymes (e.g. elastase and lysophospholipase).
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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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Vitamin B12 is transported from the enterocytes to the bone marrow by which factor?
Your Answer: Transcobalamin I (TC 1)
Correct Answer: Transcobalamin II (TC IIi)
Explanation:B12 must be attached to 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. Once the IF/B12 complex is recognized by specialized ileal receptors, it is transported into the portal circulation. The vitamin is then transferred to transcobalamin II (TC-II/B12), which serves as the plasma transporter.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 14
Correct
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Which of the following is true regarding platelets?
Your Answer: Normally have a half-life of about 8 days
Explanation:Platelets have no cell nucleus: they are fragments of cytoplasm that are derived from the megakaryocytes of the bone marrow, and then enter the circulation. They have a half life of 5-9 days.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 15
Correct
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From which of the following can niacin be synthesized in humans
Your Answer: Tryptophan
Explanation:Niacin, is also known as vitamin B3. The liver can synthesize niacin from the essential amino acid tryptophan, requiring 60 mg of tryptophan to make one mg of niacin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 16
Correct
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One of the cells of the bone marrow that are responsible for forming the various forms of differentiated blood cells are called?
Your Answer: Hematopoietic stem cell
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 are derived from mesoderm and located in the red bone marrow, which is contained in the core of most bones.
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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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Platelets are stored in this body organ.
Your Answer: Spleen
Explanation:Megakaryocyte and platelet production is regulated by thrombopoietin. Each megakaryocyte produces between 1,000 and 3,000 platelets during its lifetime. An average of 1011 platelets are produced daily in a healthy adult. Reserve platelets are stored in the spleen, and are released when needed by splenic contraction induced by the sympathetic nervous system.
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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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Question 19
Incorrect
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Question 20
Incorrect
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Why is tissue plasminogen activator (tPa) a valuable treatment used in myocardial infarction and stroke?
Your Answer: It directly lyses fibrin
Correct Answer: It forms plasmin from its inactive precursor
Explanation:tPA is a serine protease involved in the breakdown of blood clots. It functions by converting plasminogen, an inactive precursor, into plasmin, an active enzyme. Plasmin then degrades fibrin, the main protein component of blood clots, leading to clot dissolution. This mechanism is particularly valuable in the treatment of myocardial infarction (heart attack) and ischemic stroke, where timely dissolution of the clot can restore blood flow to affected tissues and reduce damage.
Therefore, the correct answer is:
- It forms plasmin from its inactive precursor
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This question is part of the following fields:
- Haematology
- Medicine
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Question 21
Correct
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The structure of haemoglobin A in adults includes
Your Answer: Haem, globin polypeptide chains α and β
Explanation:Haemoglobin A (HbA), also known as adult haemoglobin or α2β2, is the most common human haemoglobin tetramer, comprising over 97% of the total red blood cell haemoglobin. It consists of two alpha chains and two beta chains.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 22
Correct
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Where is Vitamin B 12 absorbed?
Your 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 23
Incorrect
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Question 24
Incorrect
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5-methyltetrahydrofolate (Methyl THF) is converted to THF with the help of which of the following?
Your Answer: Dihydrofolate reductase
Correct Answer: B 12
Explanation:MTR, also known as methionine synthase, is a methyltransferase enzyme, which uses the Vitamin B12 to transfer a methyl group from 5-methyltetrahydrofolate to homocysteine, thereby generating tetrahydrofolate (THF) and methionine. This functionality is lost in vitamin B12 deficiency, resulting in an increased homocysteine level and the trapping of folate as 5-methyl-tetrahydrofolate, from which THF (the active form of folate) cannot be recovered. THF plays an important role in DNA synthesis so reduced availability of THF results in ineffective production of cells with rapid turnover, in particular red blood cells, and also intestinal wall cells which are responsible for absorption.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 25
Incorrect
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Inactive cellular marrow is called
Your Answer: White 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 26
Correct
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What is the function of Activated protein C?
Your Answer: Inactivates factor Va
Explanation:Activated Protein C (APC) is a crucial protein in the regulation of blood coagulation. Its primary functions include:
- Inactivating Factor Va: APC inactivates Factor Va, which is a cofactor for the conversion of prothrombin to thrombin by Factor Xa. By inactivating Factor Va, APC reduces thrombin formation, thereby acting as an anticoagulant.
- Inactivating Factor VIIIa: APC also inactivates Factor VIIIa, another cofactor that assists Factor IXa in the conversion of Factor X to Factor Xa. This further contributes to its anticoagulant effect.
These actions help to regulate blood clotting and prevent excessive thrombosis.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 27
Incorrect
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With regards to splenic micro-architecture which is not contained within the red pulp
Your Answer: Red blood cells
Correct Answer: Malpighian corpuscles
Explanation:Red pulp is responsible for mechanical filtration of red blood cells and is composed of sinusoids, which are filled with blood, splenic cords of reticular fibers and a marginal zone bordering on white pulp. White pulp provides an 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 (PALS), rich in T-lymphocytes.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 28
Correct
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Regarding transportation of iron in the body, the process in which iron is transported from the enterocyte into the blood occurs using which transporter protein:
Your Answer: Ferroportin
Explanation:Divalent metal transporter 1 (DMT1) transport several divalent metals including iron across the enterocyte’s cell membrane into the cell. The cell can then release it into the body via the only known iron exporter in mammals, ferroportin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 29
Correct
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The process in which tissue thromboplastin activates factor VII is best known as:
Your Answer: The extrinsic pathway
Explanation:In the tissue factor pathway (extrinsic), following damage to the blood vessel, FVII leaves the circulation and comes into contact with tissue factor (TF) expressed on tissue-factor-bearing cells (stromal fibroblasts and leukocytes), forming an activated complex (TF-FVIIa).
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This question is part of the following fields:
- Haematology
- Medicine
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Question 30
Incorrect
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Which statement is correct about the clinical state of methemoglobinemia?
Your Answer: It is due to carbon monoxide reacting with haemoglobin.
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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SESSION STATS - PERFORMANCE PER SPECIALTY
