11β-hydroxylase deficiency differential diagnosis: Difference between revisions
No edit summary |
No edit summary |
||
| Line 3: | Line 3: | ||
{{CMG}}; {{AE}} {{Ammu}} | {{CMG}}; {{AE}} {{Ammu}} | ||
==Overview== | ==Overview== | ||
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency must be differentiated from other diseases that cause | 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== | ==Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases== | ||
* Adrenal crisis | * Adrenal crisis | ||
Revision as of 18:04, 28 January 2016
|
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
|
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
11β-hydroxylase deficiency differential diagnosis On the Web |
|
American Roentgen Ray Society Images of 11β-hydroxylase deficiency differential diagnosis |
|
11β-hydroxylase deficiency differential diagnosis in the news |
|
Directions to Hospitals Treating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency |
|
Risk calculators and risk factors for 11β-hydroxylase deficiency differential diagnosis |
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