11β-hydroxylase deficiency differential diagnosis

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters
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Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

Overview

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency must be differentiated from other diseases that cause clinical features, such as adrenal crisis, conn syndrome, gastric outlet obstruction, congenital adrenal hyperplasia due to 17-hydroxylase deficiency, congenital adrenal hyperplasia due to 21-hydroxylase deficiency, hypertension, hypokalemia, hypomagnesemia, infertility, polycystic ovarian syndrome, malignant hypertension, Stein-Leventhal syndrome, and viral gastroenteritis.

Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases

• Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency must be differentiated from following diseases:

• Adrenal crisis
• Conn syndrome
• Gastric outlet obstruction
• Congenital adrenal hyperplasia due to 17-hydroxylase deficiency
• Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
• Congenital hypertrophic pyloric stenosis
• Hypertension
• Hypokalemia
• Hypomagnesemia
• Iatrogenic cushing syndrome
• Infertility
• Malignant hypertension
• Male infertility
• Polycystic ovarian syndrome
• Primary aldosteronism
• Stein-Leventhal syndrome
• Viral gastroenteritis

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