Endocrinology Exam Questions

Questions 54

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Endocrinology Exam Questions Questions

Question 1 of 5

Tetany is characterized by all of the following signs except:

Correct Answer: C

Rationale: Tetany is a condition characterized by involuntary muscle spasms and contractions due to low levels of calcium in the blood. The signs associated with tetany include Trousseau's sign, which is the carpal spasm elicited by inflating a blood pressure cuff above systolic pressure, and Chvostek's sign, which is the facial muscle spasm elicited by tapping on the facial nerve. Peroneal sign is not specifically associated with tetany but can be seen in conditions like peroneal nerve injury. Erb's sign, on the other hand, is not a recognized sign of tetany. It is associated with Erb's palsy, a condition resulting from injury to the brachial plexus nerves, typically during childbirth. Tinel's sign, which is a tingling sensation elicited by tapping over a compressed nerve, is also not a characteristic sign of tetany.

Question 2 of 5

Which of the following are causes of nephrogenic diabetes insipidus?

Correct Answer: B

Rationale: Nephrogenic diabetes insipidus (NDI) is a condition where the kidneys are unable to respond to antidiuretic hormone (ADH) as they should, leading to excessive urination and extreme thirst. One of the main causes of nephrogenic diabetes insipidus is the use of certain medications, with lithium being the most common culprit. Lithium can interfere with the kidney's response to ADH, resulting in decreased water reabsorption and the characteristic symptoms of diabetes insipidus. Other causes of NDI can include genetic mutations affecting the vasopressin receptor gene or other underlying conditions such as hypercalcemia, hypokalemia, or obstructive uropathy.

Question 3 of 5

The receptors for non-steroid peptide hormones are found on the ______.

Correct Answer: A

Rationale: The receptors for non-steroid peptide hormones are typically found on the plasma membrane of target cells. These hormones are large or polar molecules that cannot easily diffuse through the cell membrane. Instead, they bind to specific receptors on the cell surface, initiating signaling pathways that eventually lead to changes within the cell. Once the peptide hormone binds to its receptor on the plasma membrane, secondary messenger systems are activated to relay the signal into the cell and initiate the appropriate cellular response. This distinct mechanism of action highlights the importance of the plasma membrane as the location of receptors for non-steroid peptide hormones.

Question 4 of 5

All the following are effects of hypercalcemia except

Correct Answer: C

Rationale: Hypercalcemia refers to elevated levels of calcium in the blood. The effects of hypercalcemia include increased urinary frequency (polyuria), gastrointestinal symptoms such as constipation rather than diarrhea, kidney stones (nephrolithiasis), and various cardiac abnormalities. One key cardiac abnormality associated with hypercalcemia is a prolonged QT interval rather than a shortened QT interval. Prolongation of the QT interval can predispose individuals to arrhythmias, particularly Torsades de pointes. Therefore, the correct answer is C, as a shortened QT interval is not a typical effect of hypercalcemia.

Question 5 of 5

Commonest enzymatic defect for development of congenital adrenal hyperplasia is:

Correct Answer: A

Rationale: C-21 hydroxylase deficiency is the most common enzymatic defect leading to the development of congenital adrenal hyperplasia (CAH). This enzyme is necessary for the synthesis of cortisol and aldosterone in the adrenal glands. When there is a deficiency in C-21 hydroxylase, the pathway is shifted towards the production of androgens instead of cortisol and aldosterone, leading to excess androgen production. This results in the characteristic features of CAH, such as ambiguous genitalia in females and virilization in both males and females. Other enzyme deficiencies listed in the choices can also lead to different types of CAH but are less common compared to C-21 hydroxylase deficiency.

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