11β-hydroxylase deficiency differential diagnosis: Difference between revisions
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==Overview== | ==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. | 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== | ||
* Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency must be differentiated from following diseases: | * Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency must be differentiated from following diseases: | ||
:* Adrenal crisis<ref> Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016</ref> | :* [[Adrenal crisis]]<ref> Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016</ref> | ||
:* Conn syndrome | :* [[Conn syndrome]] | ||
:* Gastric outlet obstruction | :* [[Gastric outlet obstruction]] | ||
:* Congenital adrenal hyperplasia due to 17-hydroxylase deficiency | :* [[Congenital adrenal hyperplasia due to 17-hydroxylase deficiency]] | ||
:* Congenital adrenal hyperplasia due to 21-hydroxylase deficiency | :* [[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]] | ||
:* Congenital hypertrophic pyloric stenosis | :* [[Congenital hypertrophic pyloric stenosis]] | ||
:* Hypertension | :* [[Hypertension]] | ||
:* Hypokalemia | :* [[Hypokalemia]] | ||
:* Hypomagnesemia | :* [[Hypomagnesemia]] | ||
:* Iatrogenic | :* Iatrogenic cushing syndrome | ||
:* Infertility | :* [[Infertility]] | ||
:* Malignant | :* [[Malignant hypertension]] | ||
:* Male | :* Male infertility | ||
:* Polycystic | :* [[Polycystic ovarian syndrome]] | ||
:* Primary | :* [[Primary aldosteronism]] | ||
:* Stein-Leventhal syndrome | :* [[Stein-Leventhal syndrome]] | ||
:* Viral | :* [[Viral gastroenteritis]] | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Templates]] | [[Category:Templates]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
Revision as of 20:36, 29 January 2016
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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[1]
- 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
References
- ↑ Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016