Thyrotoxicosis may be featured by all except:
- A. Myopathy
- B. Pretibial myxoedema
- C. Hypernatraemia
- D. Atrial fibrillation
Correct Answer: A
Rationale: Thyrotoxicosis, also known as hyperthyroidism, is a condition characterized by excessive thyroid hormone production by the thyroid gland. Symptoms of thyrotoxicosis can include weight loss, heat intolerance, tremors, hyperactivity, and fatigue. While musculoskeletal symptoms such as weakness and tremors are common in thyrotoxicosis, true myopathy (muscle disease) is not a typical feature of the condition. Therefore, myopathy is the correct choice among the given options.
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All of the following are potential signs or symptoms of growth hormone deficiency except:
- A. Abnormal lipid profile
- B. Atherosclerosis
- C. Increased bone mineral density
- D. Left ventricular dysfunction
Correct Answer: C
Rationale: Growth hormone deficiency (GHD) is commonly associated with decreased bone mineral density, leading to an increased risk of fractures and osteoporosis. Therefore, increased bone mineral density would not typically be a sign or symptom of GHD. On the other hand, abnormal lipid profile, atherosclerosis, and left ventricular dysfunction are all potential signs or symptoms of GHD. Abnormal lipid profile can manifest as increased levels of LDL cholesterol and decreased levels of HDL cholesterol. Atherosclerosis, the buildup of plaque in the arteries, can occur in individuals with GHD due to the impact on lipid metabolism. Left ventricular dysfunction may also be seen in individuals with GHD due to the role of growth hormone in cardiac function and structure.
The triad of hyponatraemia, haemodilution and urine hypertonic to plasma suggest diagnosis of:
- A. Nephrotic syndrome
- B. SIADH
- C. Nephrogenic diabetes insipidus
- D. Addison's disease
Correct Answer: B
Rationale: The triad of hyponatremia (low sodium levels in the blood), haemodilution (increased plasma volume), and urine hypertonic to plasma (high urine osmolality compared to blood osmolality) is characteristic of Syndrome of Inappropriate Antidiuretic Hormone (SIADH). In SIADH, there is excessive release of antidiuretic hormone (ADH), also known as vasopressin, leading to water retention by the kidneys and dilutional hyponatremia. This condition results in the body holding onto water, causing hyponatremia and dilution of the blood. The urine being hypertonic compared to plasma indicates that the kidneys are reabsorbing water effectively and concentrating the urine.
All are features of diabetic ketoacidosis except:
- A. Hyperthermia
- B. Drowsiness
- C. Dehydration
- D. Air hunger
Correct Answer: A
Rationale: Hyperthermia is not a typical feature of diabetic ketoacidosis (DKA). DKA is typically characterized by high blood sugar levels, ketone accumulation, metabolic acidosis, dehydration, drowsiness, and, in severe cases, unconsciousness. Common symptoms include drowsiness, dehydration, and air hunger (deep and rapid breathing). However, hyperthermia, which refers to an elevated body temperature, is not a characteristic typically associated with DKA. It is important to monitor and manage DKA promptly as it is a serious complication of diabetes that requires immediate medical attention.
Persistent muscular weakness is characteristic of:
- A. Conn's syndrome
- B. Acromegaly
- C. Hyperparathyroidism
- D. Myxoedema
Correct Answer: D
Rationale: Persistent muscular weakness is characteristic of myxoedema, which is severe hypothyroidism. Myxoedema can lead to general weakness and fatigue, as thyroid hormones play a crucial role in controlling metabolism and energy production in the body. Other symptoms of myxoedema include cold intolerance, weight gain, dry skin, and hair loss. Conn's syndrome (hyperaldosteronism) is characterized by hypertension and low potassium levels, not persistent muscular weakness. Acromegaly is a condition resulting from excess growth hormone production, leading to enlarged body parts and metabolic changes but not specifically muscular weakness. Hyperparathyroidism is associated with high levels of parathyroid hormone, which can lead to bone weakening and calcium imbalance, but it is not typically a primary cause of muscular weakness.
All of the following are featured by dermal hyperpigmentation except:
- A. Conn's syndrome
- B. Bronchogenic carcinoma
- C. Addison's disease
- D. Haemochromatosis
Correct Answer: A
Rationale: Dermal hyperpigmentation, also known as hyperpigmentation of the skin, is commonly associated with conditions such as Addison's disease, hemochromatosis, and bronchogenic carcinoma. In Addison's disease, there is increased production of melanin due to elevated levels of adrenocorticotropic hormone (ACTH) which stimulates melanocytes. Hemochromatosis can cause hyperpigmentation due to excess iron deposits in the skin. Bronchogenic carcinoma can lead to a condition known as acanthosis nigricans, characterized by dark, velvety discoloration of the skin primarily around the neck and armpits. However, Conn's syndrome, which is a primary aldosteronism resulting from an adrenal adenoma or hyperplasia, is not typically associated with dermal hyperpigmentation.
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