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Question 1
Correct
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Which of the following conditions is associated with eosinophilia?
Your Answer: Ascaris
Explanation:Eosinophilia can be idiopathic (primary) or, more commonly, secondary to another disease. In the Western World, allergic or atopic diseases are the most common causes, especially those of the respiratory or integumentary systems. In the developing world, parasites are the most common cause e.g. Ascaris
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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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In the clotting mechanism, activation of factor IX can occur through the direct actions of:
Your Answer: Factor XIa & XIIa
Correct Answer: Factor VIIa & XIa
Explanation:Factor IX is processed to remove the signal peptide, glycosylated and then cleaved by factor XIa (of the contact pathway) or factor VIIa (of the tissue factor pathway). When activated into factor IXa, in the presence of Ca2+, membrane phospholipids, and a Factor VIII cofactor, it hydrolyses one arginine-isoleucine bond in factor X to form factor Xa. Factor IX is inhibited by antithrombin.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 3
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 4
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 5
Correct
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Question 6
Incorrect
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Vitamin K deficiency can be found in which of the following condition?
Your Answer: Intestinal bacterial overgrowth
Correct Answer: Cholestatic jaundice
Explanation:Vitamin K1-deficiency may occur by disturbed intestinal uptake (such as would occur in a bile duct obstruction), by therapeutic or accidental intake of a vitamin K1-antagonist such as warfarin, or, very rarely, by nutritional vitamin K1 deficiency.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 7
Correct
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Choose the correct statement regarding the protein C/S system?
Your 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 8
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 9
Correct
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Question 10
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 11
Incorrect
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Which of the following is a function of Vitamin C?
Your Answer: Iron transport across the enterocytes
Correct Answer: Hydroxylation of proline to hydroxyproline for collagen synthesis
Explanation:Vitamin C acts as an electron donor for eight different enzymes: Three enzymes (prolyl-3-hydroxylase, prolyl-4-hydroxylase, and lysyl hydroxylase) that are required for the hydroxylation of proline and lysine in the synthesis of collagen.
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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 conditions is procoagulant?
Your 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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Question 13
Correct
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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: 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
Correct
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90% of erythropoietin necessary for haemopoesis is produced by the kidneys, the remainder is formed in the?
Your Answer: Liver
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 15
Correct
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Which one of the following is necessary to activate plasminogen to plasmin?
Your Answer: tPA
Explanation:In circulation, plasminogen adopts a closed, activation resistant conformation. Upon binding to clots, or to the cell surface, plasminogen adopts an open form that can be converted into active plasmin by a variety of enzymes, including tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, and factor XII (Hageman factor).
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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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The following play a role in regulation of intestinal iron absorption except:
Your Answer: Urinary iron excretion rate
Explanation:The human body’s rate of iron absorption appears to respond to a variety of interdependent factors, including total iron stores, dietary intake, the extent to which the bone marrow is producing new red blood cells, the concentration of haemoglobin in the blood, and the oxygen content of the blood. Classic examples of genetic iron overload includes hereditary hemochromatosis (HH) and the more severe disease juvenile hemochromatosis (JH).
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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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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 18
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 19
Incorrect
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Which vitamin plays a major role in the metabolism of many amino acids?
Your Answer: Vitamin B3
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 20
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 21
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 22
Correct
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All of the following are Vitamin K-dependent clotting factors except:
Your Answer: Factor XI
Explanation:Activated Vitamin K is used to gamma carboxylate (and thus activate) certain enzymes involved in coagulation: Factors II, VII, IX, X, and protein C and protein S. Inability to activate the clotting cascade via these factors leads to the bleeding symptoms
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This question is part of the following fields:
- Haematology
- Medicine
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Question 23
Correct
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Where is retinol mainly stored?
Your Answer: Liver
Explanation:Vitamin A is a group of unsaturated nutritional organic compounds that includes retinol, retinal, retinoic acid, and several provitamin A carotenoids (most notably beta-carotene). The liver stores a multitude of substances, including glucose (in the form of glycogen), vitamin A (1–2 years’ supply), vitamin D (1–4 months’ supply), vitamin B12 (3–5 years’ supply), vitamin K, iron, and copper.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 24
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 25
Correct
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Iron absorption occurs primarily in which part of the GIT?
Your Answer: Duodenum
Explanation:Like most mineral nutrients, the majority of the iron absorbed from digested food or supplements is absorbed in the duodenum by enterocytes of the duodenal lining.
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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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Question 27
Correct
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Synthesis of haem for haemoglobin occurs in the?
Your 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 28
Correct
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Inactive cellular marrow is called
Your 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 29
Correct
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Question 30
Incorrect
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With regard to the spleen which of the following has the correct match?
Your Answer: Marginal zone - B lymphocytes
Correct 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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