In classic CAH due to 21-hydroxylase deficiency, which combination of hormone production occurs?

Study for the Disorders of the Adrenal Gland Test. Use flashcards and multiple-choice questions, each with hints and explanations. Prepare for your exam!

Multiple Choice

In classic CAH due to 21-hydroxylase deficiency, which combination of hormone production occurs?

Explanation:
In classic CAH from 21-hydroxylase deficiency, the block in the adrenal steroid pathway reduces production of both cortisol and aldosterone, while precursors are shunted into androgen synthesis. So cortisol and aldosterone are deficient, and androgens are elevated due to increased ACTH drive and enzyme block. This combination—deficient cortisol and aldosterone with excess androgens—best fits the scenario. The other patterns don’t match: aldosterone is not increased (it’s decreased), cortisol is not in excess (it’s deficient), and androgens are not normal.

In classic CAH from 21-hydroxylase deficiency, the block in the adrenal steroid pathway reduces production of both cortisol and aldosterone, while precursors are shunted into androgen synthesis. So cortisol and aldosterone are deficient, and androgens are elevated due to increased ACTH drive and enzyme block. This combination—deficient cortisol and aldosterone with excess androgens—best fits the scenario.

The other patterns don’t match: aldosterone is not increased (it’s decreased), cortisol is not in excess (it’s deficient), and androgens are not normal.

Subscribe

Get the latest from Passetra

You can unsubscribe at any time. Read our privacy policy