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==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
 
* 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==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 00:20, 28 January 2016

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters

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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

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

References


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