Questions 9

ATI RN

ATI RN Test Bank

Endocrinology Exam Questions and Answers Questions

Question 1 of 5

All of the following are potential signs or symptoms of growth hormone deficiency except:

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.

Question 2 of 5

Calcification of basal ganglia is seen in:

Correct Answer: A

Rationale: Primary hyperparathyroidism is a condition characterized by the overproduction of parathyroid hormone (PTH) by the parathyroid glands, leading to elevated levels of calcium in the blood. This excessive calcium can cause calcification in various tissues, including the basal ganglia of the brain. The calcification of the basal ganglia in primary hyperparathyroidism is a well-known radiological finding and can be visualized on imaging studies such as CT scans or MRI. Hypoparathyroidism, on the other hand, is characterized by low levels of PTH and results in decreased serum calcium levels, making it an unlikely cause of basal ganglia calcification. Secondary hyperparathyroidism is associated with chronic kidney disease and is also characterized by high PTH levels, but basal ganglia calcification is not a typical manifestation of this condition. Milk-alkali syndrome is a disorder characterized by excessive intake of

Question 3 of 5

Persistent muscular weakness is characteristic of:

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.

Question 4 of 5

Which of the following is not a symptom of Cushing's syndrome?

Correct Answer: D

Rationale: Weight gain is a common symptom of Cushing's syndrome due to the excessive production of cortisol, a hormone that regulates metabolism and fat storage. The other symptoms listed, such as easy bruising, acne, and stretch marks, are also characteristic features of Cushing's syndrome. However, weight loss is typically not associated with this condition. In fact, individuals with Cushing's syndrome often experience unexplained and rapid weight gain, especially in the face, abdomen, and upper back (resulting in a characteristic "buffalo hump" appearance), rather than weight loss.

Question 5 of 5

Which of the following are not causes of neurogenic diabetes insipidus?

Correct Answer: D

Rationale: Neurogenic diabetes insipidus is due to a deficiency in vasopressin (antidiuretic hormone, ADH) production in the hypothalamus or a failure of proper vasopressin release from the posterior pituitary. Causes of neurogenic DI typically involve factors affecting vasopressin synthesis, storage, or release. However, mutations in the vasopressin gene itself would be a cause of genetic forms of diabetes insipidus, not neurogenic diabetes insipidus. Common causes of neurogenic diabetes insipidus include traumatic brain injury, brain tumors, pituitary adenomas, meningitis, and Sheehan's syndrome.

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