Nokea
Tall stature is not characteristic of:
- A. Klinefelter's syndrome
- B. Homocystinuria
- C. Marfan's syndrome
- D. Turner's syndrome
Correct Answer: D
Rationale: Turner's syndrome is a genetic condition that affects females and is characterized by short stature and other physical abnormalities due to the absence of part or all of one of the X chromosomes. Therefore, tall stature is not characteristic of Turner's syndrome.
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Effect of diabetes on foetus includes all except:
- A. Microsomia
- B. Hyperbilirubinaemia
- C. Stillbirth
- D. Open neural tube defect
Correct Answer: B
Rationale: Hyperbilirubinemia is not a common effect of diabetes on the fetus. The correct effects of diabetes on the fetus include:
Prolonged ingestion of iodine can produce goiter, and is known as:
- A. Jod-Basedow effect
- B. Sick euthyroid syndrome
- C. Wolf-Chaikoff effect
- D. Thyrotoxicosis factitia
Correct Answer: C
Rationale: The prolonged ingestion of iodine causing goiter is known as the Wolf-Chaikoff effect. This phenomenon occurs when high levels of iodine cause a temporary inhibition of thyroid hormone synthesis, resulting in a decrease in thyroid hormone production. In some individuals, this can lead to the development of a goiter due to the lack of thyroid hormone feedback regulation. It is important to note that the Wolf-Chaikoff effect typically resolves on its own as the thyroid gland adapts to the increased iodine levels over time.
Aldosterone:
- A. is synthesized in the zona fasciculata.
- B. is deficient in Conn's syndrome.
- C. is independent of ACTH.
- D. is suppressed by elevated potassium.
Correct Answer: D
Rationale: Aldosterone is a hormone produced in the zona glomerulosa of the adrenal cortex, not the zona fasciculata (Choice A is incorrect). Conn's syndrome, also known as primary hyperaldosteronism, is characterized by excess aldosterone secretion, not a deficiency (Choice B is incorrect). Aldosterone production is under the control of the renin-angiotensin-aldosterone system, which is stimulated by factors such as low blood pressure, low blood volume, and high potassium levels. Elevated potassium in the blood directly suppresses aldosterone production by the adrenal glands, serving as a negative feedback mechanism to maintain electrolyte balance (Choice D is correct). The synthesis of aldosterone also requires cholesterol as the precursor, rather than pregnenolone (Choice E is incorrect). Lastly, aldosterone production is regulated in part by ACTH (adrenocorticotropic hormone), as it can enhance the effects of
Commonest enzymatic defect for development of congenital adrenal hyperplasia is:
- A. C-21 hydroxylase deficiency
- B. 3b dehydrogenase deficiency
- C. C-11 hydroxylase deficiency
- D. C-17 hydroxylase deficiency
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.
Which age group does acromegaly most commonly affect?
- A. 30-50 years
- B. 10-25 years
- C. 55-70 years
- D. 25-40 years
Correct Answer: A
Rationale: Acromegaly most commonly affects individuals in the age group of 30-50 years. This condition is typically diagnosed in adults between these ages. Acromegaly is often caused by the overproduction of growth hormone in adults, which leads to excessive bone growth and tissue expansion. While acromegaly can develop at any age, it is more commonly seen in adults within the 30-50 age range.