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  • Question 1 - What muscles are responsible for dorsiflexion of the ankle joint? ...

    Incorrect

    • What muscles are responsible for dorsiflexion of the ankle joint?

      Your Answer: Tibialis posterior

      Correct Answer: Tibialis anterior

      Explanation:

      Muscles Involved in Ankle and Toe Movements

      The tibialis anterior muscle is responsible for dorsiflexion of the ankle joint, which means it helps lift the foot upwards towards the shin. On the other hand, the tibialis posterior, soleus, and gastrocnemius muscles are involved in plantar flexion, which is the movement of pointing the foot downwards. These muscles work together to push the foot off the ground during walking or running.

      Another muscle involved in foot movement is the flexor digitorum longus, which is responsible for flexion of the second to fifth toes. This muscle helps curl the toes downwards towards the sole of the foot. All of these muscles play important roles in the complex movements of the foot and ankle, allowing us to walk, run, jump, and perform other activities that require precise control of our lower limbs.

    • This question is part of the following fields:

      • Clinical Sciences
      27.8
      Seconds
  • Question 2 - What is the name of the muscle that performs hip flexion and knee...

    Incorrect

    • What is the name of the muscle that performs hip flexion and knee extension?

      Your Answer: Vastus Medialis

      Correct Answer: Rectus femoris

      Explanation:

      Muscles of the Hip and Knee Joints

      The rectus femoris muscle originates from the anterior inferior iliac spine and the ilium just above the acetabulum. It then inserts into the quadriceps femoris tendon. Similarly, the sartorius muscle also originates from the ilium and inserts into the quadriceps femoris tendon, but it functions to flex the leg at the knee joint. On the other hand, the iliacus and psoas major muscles only provide flexion of the hip joint. Lastly, the vastus medialis muscle is responsible for extending the knee joint. the origins and insertions of these muscles can aid in the diagnosis and treatment of hip and knee joint injuries.

    • This question is part of the following fields:

      • Clinical Sciences
      46.5
      Seconds
  • Question 3 - A 38-year-old obese woman presents to the Emergency department complaining of sharp cramping...

    Incorrect

    • A 38-year-old obese woman presents to the Emergency department complaining of sharp cramping pains in the right upper quadrant of her abdomen. The pain started this afternoon after a large meal, but she has experienced similar problems over the past few weeks and ignored them, hoping they would go away. She denies any vomiting or diarrhea and is apyrexial. Upon examination, her abdomen is soft, but there is tenderness in the right upper quadrant. Her FBC and U&Es are normal. What is the most likely diagnosis?

      Your Answer: Cholecystitis

      Correct Answer: Cholelithiasis

      Explanation:

      Cholecystitis and Other Digestive Conditions

      Cholecystitis is a condition characterized by inflammation of the gallbladder, which can cause mild fever and vomiting. On the other hand, cholelithiasis, or the presence of gallstones, can lead to cramping pains after eating as the gallbladder contracts to expel bile. This condition is more common in women who are fair, fat, and fertile.

      Dyspepsia, or indigestion, typically causes central pain that is not severe enough to warrant a hospital visit. Gastroenteritis, which is characterized by diarrhea and vomiting, is unlikely if these symptoms are not present. Peptic ulcers, which can cause pain related to eating, are usually accompanied by vomiting and bloating.

      these different digestive conditions can help individuals identify and seek appropriate treatment for their symptoms. It is important to consult a healthcare professional for an accurate diagnosis and treatment plan.

    • This question is part of the following fields:

      • Clinical Sciences
      26.7
      Seconds
  • Question 4 - Which enzyme is likely to be dysfunctional in patients with chronic granulomatous disease,...

    Correct

    • Which enzyme is likely to be dysfunctional in patients with chronic granulomatous disease, resulting in their inability to efficiently eliminate bacteria after ingestion by macrophages?

      Your Answer: NADPH oxidase

      Explanation:

      Granulocyte Bacterial Killing Mechanisms

      Granulocytes have a unique way of killing bacteria. Although it is a rare condition, it exemplifies the bacterial killing mechanisms of granulocytes. Once a bacterium is ingested, granulocytes fuse the phagosome with lysosomes that contain proteolytic enzymes. Additionally, they produce oxygen radicals (O2-) that can react with nitric oxide (forming ONOO-), both of which are harmful to bacteria. This process is known as the respiratory burst and utilises the enzyme NADPH oxidase. Patients who have a loss of function of NADPH oxidase are unable to effectively kill bacteria, which leads to the formation of granulomas, sealing off the infection. These patients are immunosuppressed.

      In contrast, a C5-convertase is a complex of proteins involved in the complement cascade. Carbonic anhydrase catalyses the formation of carbonic acid from water and CO2. Lactate dehydrogenase converts pyruvate into lactic acid. TDT is an enzyme that is used to insert mutations into somatic DNA during the formation of the B cell and T cell receptor. Each of these processes has a unique function in the body, but the granulocyte bacterial killing mechanism is particularly fascinating due to its ability to effectively combat bacterial infections.

    • This question is part of the following fields:

      • Clinical Sciences
      16.4
      Seconds
  • Question 5 - What is the net ATP production per glucose molecule during glycolysis? ...

    Incorrect

    • What is the net ATP production per glucose molecule during glycolysis?

      Your Answer: Net production of 6 molecules of ATP per molecule glucose

      Correct Answer: Net production of 2 molecules of ATP per molecule glucose

      Explanation:

      ATP Production during Glycolysis

      During glycolysis, two molecules of ATP are initially used up. One molecule is utilized to convert glucose to glucose 6 phosphate, while the other is used for the conversion of fructose 6 phosphate to fructose 1,6 bisphosphate. The fructose 1,6 bisphosphate is then split into two 3-carbon molecules, each of which can generate 2 molecules of ATP. As a result, for each molecule of glucose, two molecules of ATP are consumed, and four are produced, resulting in a net gain of two molecules of ATP.

      It is important to note that glycolysis does not require oxygen to function. In the absence of oxygen, the glycolysis pathway can still operate, resulting in a small net gain of ATP. However, when oxygen is available, the net ATP gain is much higher for each molecule of glucose. This is because the pyruvate generated during glycolysis can be further metabolized during the Kreb cycle and electron transfer chain.

    • This question is part of the following fields:

      • Clinical Sciences
      7.4
      Seconds
  • Question 6 - In which mediastinal region is the heart located? ...

    Correct

    • In which mediastinal region is the heart located?

      Your Answer: The middle mediastinum

      Explanation:

      The genetic basis of cystic fibrosis (CF) is a crucial factor in understanding this genetic disorder that affects the respiratory, digestive, and reproductive systems. CF is caused by mutations in a single gene located on chromosome 7, which encodes the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This protein plays a vital role in regulating the movement of salt and water in and out of cells, particularly in the lungs and pancreas.

      The likelihood of being a carrier of the CF gene is relatively high, with a chance of 1 in 20 for the general population. However, the chances of two carriers of the gene having a child with CF are much lower, at 1 in 80. This is because CF is a recessive disorder, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disease.

      Understanding the genetic basis of CF is crucial for individuals and families who may be at risk of carrying the gene. Genetic testing and counseling can help identify carriers and provide information about the risks of passing on the gene to future generations. Advances in medical treatments and therapies have improved the outlook for individuals with CF, but ongoing research is needed to develop more effective treatments and ultimately find a cure.

    • This question is part of the following fields:

      • Clinical Sciences
      9.4
      Seconds
  • Question 7 - A 70-year-old man arrives at the Emergency department displaying indications and symptoms of...

    Incorrect

    • A 70-year-old man arrives at the Emergency department displaying indications and symptoms of acute coronary syndrome. Among the following cardiac enzymes, which is the most probable to increase first after a heart attack?

      Your Answer: Troponin I

      Correct Answer: Myoglobin

      Explanation:

      Enzyme Markers for Myocardial Infarction

      Enzyme markers are used to diagnose myocardial infarction, with troponins being the most sensitive and specific. However, troponins are not the fastest to rise and are only measured 12 hours after the event. Myoglobin, although less sensitive and specific, is the earliest marker to rise. The rise of myoglobin occurs within 2 hours of the event, with a peak at 6-8 hours and a fall within 1-2 days. Creatine kinase rises within 4-6 hours, peaks at 24 hours, and falls within 3-4 days. LDH rises within 6-12 hours, peaks at 72 hours, and falls within 10-14 days. These enzyme markers are important in the diagnosis and management of myocardial infarction.

    • This question is part of the following fields:

      • Clinical Sciences
      15.4
      Seconds
  • Question 8 - How would a CT scan show the structure located posteriorly to the first...

    Incorrect

    • How would a CT scan show the structure located posteriorly to the first part of the duodenum?

      Your Answer: Superior mesenteric vessels

      Correct Answer: Portal vein

      Explanation:

      Anatomy of the Duodenum

      The duodenum, which is the first part of the small intestine, can be divided into four sections. The posterior relations of the first part of the duodenum include the portal vein, common bile duct, and gastroduodenal artery, with the inferior vena cava located behind them. The third part of the duodenum is crossed by the abdominal aorta, while the superior mesenteric vessels are an anterior relation of this section. The second part of the duodenum is where the main pancreatic duct opens, and it is also crossed by the transverse colon.

    • This question is part of the following fields:

      • Clinical Sciences
      25.8
      Seconds
  • Question 9 - A 30-year-old sailor has been diagnosed with scurvy.

    What is the underlying cause...

    Incorrect

    • A 30-year-old sailor has been diagnosed with scurvy.

      What is the underlying cause of scurvy?

      Your Answer: Vitamin B12 deficiency

      Correct Answer: Vitamin C deficiency

      Explanation:

      The Importance of Vitamins and Their Deficiencies

      Vitamins play a crucial role in maintaining the body’s overall health and well-being. Scurvy, a condition caused by a deficiency in vitamin C, is commonly observed in sailors who lack access to fresh fruits and vegetables during long sea voyages. The symptoms of scurvy include a widespread rash, bleeding mucous membranes, impaired wound healing, rough skin, fatigue, and depression. Vitamin C has several essential functions in the body, including acting as an antioxidant, reducing iron and copper, synthesizing collagen, producing energy from fats, synthesizing neurotransmitters, enhancing immune function, and acting as an antihistamine.

      Deficiencies in other vitamins can also lead to various health problems. A lack of vitamin B3 can cause diarrhea, confusion, and skin changes known as pellagra. Vitamin B12 deficiency can lead to macrocytic anemia and paresthesia. Vitamin A toxicity can cause bone pain, dizziness, and blurred vision, while vitamin D toxicity can lead to vomiting, bone pain, and increased urinary frequency. It is essential to maintain a balanced diet and ensure adequate intake of all essential vitamins to prevent deficiencies and maintain optimal health.

    • This question is part of the following fields:

      • Clinical Sciences
      10.4
      Seconds
  • Question 10 - On which continent is the prevalence of protein-energy malnutrition highest among children? ...

    Incorrect

    • On which continent is the prevalence of protein-energy malnutrition highest among children?

      Your Answer: Africa

      Correct Answer: Asia

      Explanation:

      The Global Problem of Protein-Energy Malnutrition

      Protein-energy malnutrition (PEM) is a widespread issue that affects people of all ages, but certain groups are at higher risk. Infants and children, older people, those living in areas with civil conflicts or wars, and those in areas with limited access to food or experiencing famine or drought are particularly vulnerable. Additionally, people with HIV infection, frequent infections, and poor water sanitation are also at risk. More than 70% of children with PEM live in Asia, while 26% live in Africa, and 4% in Latin America and the Caribbean. This problem is devastating and requires global attention to address the root causes and provide necessary resources to those in need.

    • This question is part of the following fields:

      • Clinical Sciences
      9.6
      Seconds
  • Question 11 - What is the full form of ATP and how is it used during...

    Correct

    • What is the full form of ATP and how is it used during exercise?

      Your Answer: Adenosine triphosphate

      Explanation:

      ATP Generation During Exercise

      During exercise, the process of muscle contraction requires the generation of ATP, which stands for adenosine triphosphate. ATP is a small molecule composed of adenine and a sugar group attached to three phosphate groups. When ATP loses a phosphate group, it becomes ADP and releases energy.

      To sustain prolonged exercise, ATP must be regenerated quickly. This is achieved through the creatine phosphate – ATP system. Creatine phosphate releases a phosphate group, which allows for the rapid regeneration of ATP from ADP. This system ensures that the muscles have a constant supply of ATP to support muscle contraction during exercise. Proper ATP generation is crucial for athletes and individuals engaging in physical activity to perform at their best.

    • This question is part of the following fields:

      • Clinical Sciences
      21.3
      Seconds
  • Question 12 - A 55-year-old obese male patient complains of a painful and swollen big toe...

    Incorrect

    • A 55-year-old obese male patient complains of a painful and swollen big toe accompanied by a mild fever. Given his history of gout, it is suspected to be the underlying cause of his current symptoms. Which blood test is the most useful in confirming a diagnosis of gout?

      Your Answer: Serum calcium pyrophosphate

      Correct Answer: Serum urate

      Explanation:

      Diagnosing Gout: the Tests and Procedures

      Gout is a condition that occurs when urate crystals accumulate in the joints, leading to an intense inflammatory response. While several blood tests can help rule out other conditions, the most specific test for gout is the measurement of serum urate levels. However, it’s important to note that gout can still be present even without hyperuricemia, especially during an acute attack. Chondrocalcinosis, a condition characterized by calcium pyrophosphate deposition, can also be mistaken for gout.

      To definitively diagnose gout, a joint aspiration procedure is necessary. This involves extracting fluid from the affected joint and examining it under polarized microscopy. Urate crystals are needle-shaped and exhibit negative birefringence, which is a key characteristic of gout.

      In summary, diagnosing gout requires a combination of blood tests and joint aspiration procedures. While serum urate levels are the most specific blood test for gout, joint aspiration is necessary to confirm the presence of urate crystals. By these tests and procedures, healthcare providers can accurately diagnose and treat gout, improving patient outcomes.

    • This question is part of the following fields:

      • Clinical Sciences
      33.9
      Seconds
  • Question 13 - A study investigated the effectiveness of a new statin therapy in preventing ischaemic...

    Correct

    • A study investigated the effectiveness of a new statin therapy in preventing ischaemic heart disease in a diabetic population. Over a period of five years, 1000 patients were randomly assigned to receive the new therapy and 1000 were given a placebo. The placebo group experienced 150 myocardial infarctions (MIs), while the group treated with the new statin had 100 infarctions. What is the yearly percentage of MIs in the diabetic population who received the placebo?

      Your Answer: 3%

      Explanation:

      Incidence of Myocardial Infarction in Diabetic Patients

      This study found that out of 1000 diabetic patients treated with a placebo over a five-year period, there were 150 cases of myocardial infarction (MI). This means that the rate of infarction in this group was 15%, which translates to an annual MI rate of 3%. These findings provide important information for healthcare professionals treating diabetic patients, as they highlight the increased risk of MI in this population. It is important for healthcare providers to be aware of this risk and take appropriate measures to prevent and manage cardiovascular complications in diabetic patients. This study emphasizes the need for continued research and development of effective prevention and treatment strategies for diabetic patients at risk for MI.

    • This question is part of the following fields:

      • Clinical Sciences
      116.4
      Seconds
  • Question 14 - What is the primary function of niacin, also known as vitamin B3? ...

    Correct

    • What is the primary function of niacin, also known as vitamin B3?

      Your Answer: Antioxidant function

      Explanation:

      The Many Functions of Niacin in the Body

      Niacin, also known as vitamin B3, plays a crucial role in various processes within the body. It acts as a cofactor in cellular reactions, aiding in the metabolism of fatty acids and steroid hormones. Additionally, niacin functions as an antioxidant, protecting the liver from free radical damage. It is also required for DNA replication and repair, as it is necessary for the synthesis of histone proteins that facilitate DNA storage, replication, and repair.

      Furthermore, niacin is involved in lipid metabolism and cholesterol regulation, with high doses of niacin being used as a lipid-lowering agent. Although not fully understood, niacin may also have a role in regulating blood sugar concentrations.

      Niacin can be obtained through the diet in two forms: nicotinic acid and nicotinamide. The body can also produce its own niacin from tryptophan, an amino acid found in protein-rich foods. With its numerous functions, niacin is an essential nutrient for maintaining optimal health.

    • This question is part of the following fields:

      • Clinical Sciences
      20.2
      Seconds
  • Question 15 - Which nerve provides the motor supply to the brachialis muscle? ...

    Correct

    • Which nerve provides the motor supply to the brachialis muscle?

      Your Answer: Radial and musculocutaneous nerve

      Explanation:

      The Brachialis Muscle: Anatomy and Innervation

      The brachialis muscle is responsible for flexing the forearm and is located in the anterior half of the humerus and intermuscular septa. It attaches to the coronoid process and tuberosity of the ulna at the elbow joint. The main nerve supply for the brachialis muscle is the musculocutaneous nerve, with C6 and radial nerve also playing a role. Additionally, the lateral part of the brachialis muscle is supplied by branches from the C7 root. Overall, the brachialis muscle is an important muscle for forearm flexion and is innervated by multiple nerves.

    • This question is part of the following fields:

      • Clinical Sciences
      23.2
      Seconds
  • Question 16 - What is the primary function of vitamin B12 within the human body? ...

    Incorrect

    • What is the primary function of vitamin B12 within the human body?

      Your Answer: Production of thyroid hormones

      Correct Answer: Synthesis of DNA

      Explanation:

      The Importance of Vitamin B12 in the Body

      Vitamin B12, also known as cobalamin, is a compound that contains cobalt and is obtained from the diet. The body has limited ability to store B12, which is why it is important to consume it regularly. Vitamin B12 works closely with folate in the body and has several important roles. It is essential for the synthesis of DNA, which allows for cell replication and tissue growth. B12 and folate are both necessary for this process. Additionally, B12 is involved in the synthesis of the myelin sheath that covers nerves and speeds up nervous transmission. It also plays a role in the metabolism of amino acids to remove harmful homocysteine, the metabolism of fats, and has an antioxidant function in association with glutathione. B12 is required for bone marrow turnover to produce healthy blood cells and platelets, which means it has some role in immunity and coagulation.

      However, a deficiency in vitamin B12 can lead to several signs and symptoms. These include megaloblastic anaemia, fatigue, breathlessness, abnormal bleeding due to reduced platelet production, impaired immune response due to reduced leucocyte production, poor function of tissues such as the skin and gut which require a high cell turnover to maintain function, and infertility. It is important to ensure that you are consuming enough vitamin B12 in your diet to avoid these deficiencies and maintain optimal health.

    • This question is part of the following fields:

      • Clinical Sciences
      72.9
      Seconds
  • Question 17 - You are in a nutrition clinic reviewing a 16-year-old boy with anorexia nervosa....

    Incorrect

    • You are in a nutrition clinic reviewing a 16-year-old boy with anorexia nervosa. He has a BMI of 15.5 kg/m2 and his weight is 70% the expected weight for height.

      How would you classify his level of malnutrition?

      Your Answer: Moderate undernutrition

      Correct Answer: Severe undernutrition

      Explanation:

      Malnutrition

      Malnutrition is a clinical condition that occurs when there is an imbalance in the energy, protein, or other components of the diet, leading to adverse effects on the body’s health. This condition encompasses undernutrition, overnutrition, and vitamin and mineral deficiencies. Undernutrition is the most common form of malnutrition and is classified based on different grading systems used worldwide. Severe undernutrition is characterized by a weight of less than 70-75% of the expected weight for age and a BMI of less than 16 kg/m2.

      To grade the severity of protein-energy malnutrition (PEM), a scale is commonly used. This scale considers the expected weight for age and BMI. A normal weight is between 90-110% of the expected weight for age and a BMI of 19-24 kg/m2. Mild undernutrition is between 85-90% of the expected weight for age and a BMI of 18-18.9 kg/m2. Moderate undernutrition is between 75-85% of the expected weight for age and a BMI of 16-17.9 kg/m2. Severe undernutrition is less than 75% of the expected weight for age and a BMI of less than 16 kg/m2.

      In summary, malnutrition is a serious condition that affects many people worldwide. the different types of malnutrition and their severity can help healthcare professionals provide appropriate treatment and interventions to improve the health outcomes of those affected.

    • This question is part of the following fields:

      • Clinical Sciences
      27.3
      Seconds
  • Question 18 - What role do chylomicrons serve in the body? ...

    Incorrect

    • What role do chylomicrons serve in the body?

      Your Answer: To move lipids from the liver to the adipocytes

      Correct Answer: To move lipids from the gut to the liver

      Explanation:

      The Role of Chylomicrons in Lipid Transport

      Chylomicrons play a crucial role in transporting lipids from the gut to the liver. When fats from the diet are absorbed in the small intestine, they form chylomicrons for transportation to the liver. These large lipoproteins are capable of transporting relatively large amounts of lipid compared to other lipoproteins.

      Lipid digestion begins in the stomach, where partial digestion and emulsification occur. As the chyle enters the small intestine, it mixes with biliary and pancreatic secretions, including pancreatic lipase and other lipases that further digest the lipid. The bile contains more cholesterol than the diet usually, and this cholesterol is also absorbed in a process known as the enterohepatic circulation.

      Digested triglyceride particles form micelles in the intestinal lumen, which aid in the absorption of the lipids into the enterocytes of the brush border. Once inside the enterocyte, triglycerides are packaged into chylomicrons, which enter the lymphatic circulation and then the bloodstream.

      Chylomicrons are modified by the enzyme lipoprotein lipase on endothelium and become chylomicron remnants. The chylomicron remnants are taken up by the liver and used to produce other lipoproteins. Overall, chylomicrons are essential for the efficient transport of lipids from the gut to the liver.

    • This question is part of the following fields:

      • Clinical Sciences
      19.8
      Seconds
  • Question 19 - What is the process by which B cells can produce epitope-specific antibodies with...

    Incorrect

    • What is the process by which B cells can produce epitope-specific antibodies with extremely high affinity through random mutations of their existing receptors?

      Your Answer: Class switching

      Correct Answer: Somatic hypermutation

      Explanation:

      The Process of B Cell Activation and Germinal Center Formation

      When an antigen activates a naïve B cell and receives appropriate signals from a Th2 CD4+ T cell, the B cell undergoes proliferation and gene mutation to form a germinal center. This process involves the formation of B-blasts and centroblasts, which insert new mutations into the variable regions of the light- and heavy-chain loci of their existing B cell receptor (BCR) through somatic hypermutation. This allows the production of a new BCR based on a receptor that is already known to bind antigen. The new BCRs are then tested against antigen by follicular dendritic cells to find a BCR with higher affinity.

      Simultaneously, class switching occurs, which refers to the exchange of heavy chain constant domain to move from IgM to any other Ig class. In the production of naïve lymphocytes in the thymus, negative and positive selection are involved. Somatic gene segment recombination is the process that allows the production of a random T cell or B cell receptor when cells are made in the bone marrow.

      Overall, the process of B cell activation and germinal center formation is a complex and intricate process that involves multiple steps and mechanisms. However, it is essential for the production of high-affinity antibodies and the development of an effective immune response.

    • This question is part of the following fields:

      • Clinical Sciences
      15.9
      Seconds
  • Question 20 - Which intrinsic muscles of the thumb are located in the thenar compartment of...

    Correct

    • Which intrinsic muscles of the thumb are located in the thenar compartment of the hand?

      Your Answer: Abductor pollicis

      Explanation:

      Muscles of the Hand

      The hand is a complex structure composed of various muscles that allow for its intricate movements. One of the compartments in the hand is the thenar compartment, which contains the abductor pollicis brevis, flexor pollicis brevis, and opponens pollicis. The adductor pollicis, although not part of the thenar group, is located deeper and more distal to the flexor pollicis brevis. Its primary function is rotation and opposition, and it is supplied by the ulnar nerve.

      Another muscle found in the hand is the first dorsal interosseous, which is located in the dorsum of the hand and innervated by the deep branch of the ulnar nerve. The first lumbrical is situated lateral to the flexor digitorum tendon of the first digit. Finally, the flexor digitorum superficialis is found in the anterior compartment of the arm.

      the muscles of the hand is crucial in diagnosing and treating hand injuries and conditions. Each muscle has a specific function and innervation, and any damage to these muscles can result in impaired hand movements. Therefore, it is essential to have a thorough knowledge of the hand’s anatomy to provide proper care and treatment.

    • This question is part of the following fields:

      • Clinical Sciences
      34.6
      Seconds

SESSION STATS - PERFORMANCE PER SPECIALTY

Clinical Sciences (6/19) 32%
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