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Question 1
Correct
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Which of the following vitamin deficiencies is associated with xerophthalmia?
Your Answer: Vitamin A
Explanation:Xerophthalmia caused by a severe vitamin A deficiency is described by pathologic dryness of the conjunctiva and cornea. The conjunctiva becomes dry, thick and wrinkled. If untreated, it can lead to corneal ulceration and ultimately to blindness as a result of corneal damage.
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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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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 3
Correct
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The actions of thrombin result directly in the release of:
Your 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
Correct
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The intrinsic pathway of coagulation is activated by which of the following?
Your Answer: Collagen fibers underlying the endothelium
Explanation:The contact activation (intrinsic) pathway begins with formation of the primary complex on collagen by high-molecular-weight kininogen (HMWK), prekallikrein, and FXII (Hageman factor).
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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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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 6
Correct
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5-methyltetrahydrofolate (Methyl THF) is converted to THF with the help of which of the following?
Your 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 7
Incorrect
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From which of the following can niacin be synthesized in humans
Your Answer: Thiamine
Correct 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 8
Correct
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Question 9
Correct
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Question 10
Incorrect
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Regarding Iron stores, which of the following contains the highest proportion of total body iron?
Your Answer: Ferritin
Correct Answer: Haemoglobin
Explanation:Most well-nourished people in industrialized countries have 4 to 5 grams of iron in their bodies. Of this, about 2.5 g is contained in the haemoglobin needed to carry oxygen through the blood, and most of the rest (approximately 2 grams in adult men, and somewhat less in women of childbearing age) is contained in ferritin complexes that are present in all cells, but most common in bone marrow, liver, and spleen.
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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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What is the average life span of neutrophils?
Your Answer: 24 hours
Explanation:The average lifespan of inactivated human neutrophils in the circulation has been reported by different approaches to be between 5 and 90 hours.
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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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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 13
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 14
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 15
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 16
Incorrect
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In the normal adult, haematopoiesis is present
Your Answer: In nearly every bone
Correct 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 17
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 18
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 19
Correct
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Which clotting factor is responsible for stabilization of the fibrin clot by formation of covalent cross-linkages?
Your 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 20
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 21
Incorrect
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In adults, the major site of haematopoiesis is?
Your Answer: The proximal ends of long bones
Correct Answer: The axial skeleton
Explanation:Bone marrow is the flexible tissue in the interior of bones. In humans, red blood cells are produced by cores of bone marrow in the heads of long bones.
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This question is part of the following fields:
- Haematology
- Medicine
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Question 22
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 23
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 24
Correct
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Which of the following foods contain Vitamin B 12?
Your 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 25
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 26
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 27
Correct
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Which of the following is a precursor to the tissue macrophage?
Your Answer: Monocyte
Explanation:Monocytes are a type of white blood cell, or leukocyte. They are the largest type of leukocyte and can differentiate into macrophages or dendritic cells.
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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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With regards to splenic micro-architecture which is not contained within the red pulp
Your 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 29
Correct
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Which of the following is matched correctly with regard to stem cells of the bone marrow?
Your 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 30
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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