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Sort elements:
21-hydroxylase deficiency
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11β-hydroxylase deficiency
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Which of the following is the diagnosis?
Let`s learn the diagnostic steps of the Cushing syndrome:
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In 21-hydroxylase deficiency level of 17-hydroxyprogesterone is ________________
Sort adrenal gland cortex zones from surface to medulla:
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Ambiguous genitalia and undescended testes in male fetuses are seen in __________
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Loss of pituitary ACTH production; low cortisol; normal aldosterone; no skin hyperpigmentation
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Abrupt withdrawal of chronic exogenous corticosteroid use; normal aldosterone; no skin hyperpigmentation
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Loss of adrenal gland function; low cortisol; low aldosterone; skin hyperpigmentation
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This is a ________
Which is the next step?
According to additional symptoms presented below which of the following is a cause?
blood pressure is high; K+ is low
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blood pressure is low; K+ is high
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Pick causes of secondary hyperaldosteronism:
Cortisol has a permissive action on catecholamines because cortisol __________
Addison disease causes _________
What is the name of the missed enzymes?
Cortisol causes leukocytosis because of:
Sort elements:
Adrenal cortex
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Adrenal medulla
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Aldosterone level in 21-hydroxylase deficiency is:
Pick factors that activate renin-angiotensin-aldosterone system (stimulate synthesis of renin):
Which of the following lung tumors is most commonly associated with paraneoplastic Cushing syndrome?
Which of the following reactions is catalyzed by 11β-hydroxylase?
Which of the following is the mechanism of action of metyrapone?
Serum level of potassium in 11β-hydroxylase deficiency is ___________
Which of the following enzymes of epinephrine synthesis is induced by cortisol?
Sort adrenogenital syndrome types:
17α-hydroxylase deficiency
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21-hydroxylase deficiency or 11β-hydroxylase deficiency
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