Endocrinology Exam Questions

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.

Correct Answer: A

Rationale: Oxytocin is a hormone produced by the hypothalamus and released by the pituitary gland. In the bloodstream, oxytocin is mostly bound to a carrier protein called neurophysin. This binding helps to protect oxytocin from being degraded too quickly in the bloodstream, thus allowing it to exert its effects on target tissues such as the uterus and mammary glands. Oxytocin plays important roles in stimulating uterine contractions during labor, facilitating milk letdown during breastfeeding, and promoting social bonding and emotional connections.

Correct Answer: B

Rationale: Small cell (oat cell) carcinoma of the lung is most commonly associated with the syndrome of inappropriate secretion of antidiuretic hormone (SIADH). This paraneoplastic syndrome occurs in patients with small cell lung cancer due to the production of antidiuretic hormone (ADH) by the tumor cells. The excessive release of ADH leads to water retention and dilutional hyponatremia, causing symptoms such as nausea, confusion, seizures, and potentially life-threatening complications. Other types of lung cancer, such as squamous cell carcinoma, large cell carcinoma, and adenocarcinoma, are less commonly associated with SIADH.

Correct Answer: B

Rationale: Conn's syndrome, also known as primary hyperaldosteronism, is characterized by excess production of aldosterone by the adrenal glands. This leads to increased sodium retention and potassium excretion in the kidneys. As a result, patients with Conn's syndrome typically present with hypokalemia (low potassium levels), not hyperkalemia (high potassium levels). The other features of Conn's syndrome include alkalosis (metabolic), muscle cramps, and severe systemic hypertension.

Correct Answer: D

Rationale: Parathyroid hormone (PTH) is a hormone produced by the parathyroid glands in response to low blood calcium levels. Its main function is to raise calcium levels in the blood by acting on the bones, kidneys, and intestines. PTH stimulates the release of calcium from the bones, enhances the absorption of calcium by the intestines, and promotes the reabsorption of calcium by the kidneys. Therefore, it is secreted in increased amounts when blood calcium levels are below normal in order to maintain overall calcium balance in the body.