11β-hydroxylase deficiency differential diagnosis
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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
- 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