21-hydroxylase deficiency differential diagnosis: Difference between revisions

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{| class="wikitable"
{| class="wikitable"
!Disease name
!Disease name
!Elevated
!Steroid status
Steroids
!Other laboratory
!Decreased steroids
!Androgen status
!Important distinguishing findings
!Important distinguishing findings
|-
|-
|Classic type of 21-hydroxylase deficiency
|Classic type of 21-hydroxylase deficiency
|17-OHP  
|Increased:
Progesterone
* 17-OHP  
Androstenedione
* Progesterone
DHEA
* Androstenedione
|Aldosterone
* DHEA
Corticosterone (salt-wasting)
Decreased:
Cortisol (simple virilizing)
* Aldosterone
* Corticosterone (salt-wasting)
* Cortisol (simple virilizing)
|
|
|-
|-
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]]
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]]
|DOC
|Increased:
11-Deoxy-
* DOC
cortisol
* 11-Deoxy-
|Cortisol
* cortisol
Corticosterone
Decreased:
Aldosterone  
* Cortisol
* Corticosterone
* Aldosterone  
|
|
|-
|-
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]]
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]]
|DOC
|Increased:
Corticosterone
* DOC
Progesterone
* Corticosterone
|Cortisol
* Progesterone
Aldosterone
Decreased:
*Cortisol
* Aldosterone
|
|
|-
|-
|3β-Hydroxysteroid Dehydrogenase  
|3β-Hydroxysteroid Dehydrogenase  
|DHEA
|Increased:
17-OH pregneno-lone  
* DHEA
Pregnenolone
* 17-OH pregneno-lone  
|Cortisol
* Pregnenolone
Aldosterone
Decreased:
* Cortisol
* Aldosterone
|
|
|-
|-
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|-
|-
|Non-classic type of 21-hydroxylase deficiency
|Non-classic type of 21-hydroxylase deficiency
|17-OHP  
|Increased:
Exaggerated androstene-dione, DHEA, and 17-OHP  
* 17-OHP  
response  
* Exaggerated androstene-dione, DHEA, and 17-OHP  
to ACTH  
response to ACTH  
|None
|
|
|-
|-
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]]
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]]
|DOC
|Increased:
11-Deoxy-
* DOC
cortisol
* 11-Deoxy-
|Cortisol
* cortisol
Corticosterone
Decreased:
Aldosterone  
* Cortisol
* Corticosterone
* Aldosterone  
|
|
|-
|-
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]]
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]]
|DOC
|Increased:
Corticosterone
* DOC
Progesterone
* Corticosterone
|Cortisol
* Progesterone
Aldosterone
Decreased:
*Cortisol
* Aldosterone
|
|
|-
|-
|3β-Hydroxysteroid Dehydrogenase  
|3β-Hydroxysteroid Dehydrogenase  
|DHEA
|Increased:
17-OH pregneno-lone  
* DHEA
Pregnenolone
* 17-OH pregneno-lone  
|Cortisol
* Pregnenolone
Aldosterone
Decreased:
* Cortisol
* Aldosterone
|
|
|-
|-
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* Polycystic ovaries in sonography
* Polycystic ovaries in sonography
* Obesity  
* Obesity  
* PCOS is the most common cause of hirsutism in women
* No evidence another diagnosis
|-
|-
|Adrenal tumors
|Adrenal tumors
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|
|
|
|
|
* Older age
* Rapidly progressive symptoms
|-
|-
|Ovarian virilizing tumor
|Ovarian virilizing tumor
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|
|
|
|
|
* Older age
* Rapidly progressive symptoms
|-
|-
|Cushing's syndrome.
|Cushing's syndrome.
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|-
|-
|hyperprolactinemia
|hyperprolactinemia
|
|
|
|
|
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== References ==
== References ==
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{{Reflist|2}}
{{WikiDoc Help Menu}}
{{WikiDoc Sources}}
[[Category:Disease]]
[[Category:Pediatrics]]
[[Category:Endocrinology]]
[[Category:Genetic disorders]]
[[Category:Intersexuality]]

Revision as of 19:44, 14 July 2017

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters

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Overview

Historical Perspective

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Differentiating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other Diseases

Epidemiology and Demographics

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Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]

Overview

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from 11-β hydroxylase deficiency, 17-α hydroxylase deficiency, androgen insensitivity syndrome, polycystic ovarian syndrome, and adrenal tumor.

Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency classic type must be differentiated from diseases that cause ambiguous genitalia:

Disease name Steroid status Other laboratory Important distinguishing findings
Classic type of 21-hydroxylase deficiency Increased:
  • 17-OHP
  • Progesterone
  • Androstenedione
  • DHEA

Decreased:

  • Aldosterone
  • Corticosterone (salt-wasting)
  • Cortisol (simple virilizing)
11-β hydroxylase deficiency Increased:
  • DOC
  • 11-Deoxy-
  • cortisol

Decreased:

  • Cortisol
  • Corticosterone
  • Aldosterone
17-α hydroxylase deficiency Increased:
  • DOC
  • Corticosterone
  • Progesterone

Decreased:

  • Cortisol
  • Aldosterone
3β-Hydroxysteroid Dehydrogenase Increased:
  • DHEA
  • 17-OH pregneno-lone
  • Pregnenolone

Decreased:

  • Cortisol
  • Aldosterone
Gestational hyperandrogenism

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Non-classic type must be differentiated from diseases that cause virilization and hirsutism in female:

Disease name Elevated

Steroids

Decreased steroids Androgen status Important distinguishing findings
Non-classic type of 21-hydroxylase deficiency Increased:
  • 17-OHP
  • Exaggerated androstene-dione, DHEA, and 17-OHP

response to ACTH

11-β hydroxylase deficiency Increased:
  • DOC
  • 11-Deoxy-
  • cortisol

Decreased:

  • Cortisol
  • Corticosterone
  • Aldosterone
17-α hydroxylase deficiency Increased:
  • DOC
  • Corticosterone
  • Progesterone

Decreased:

  • Cortisol
  • Aldosterone
3β-Hydroxysteroid Dehydrogenase Increased:
  • DHEA
  • 17-OH pregneno-lone
  • Pregnenolone

Decreased:

  • Cortisol
  • Aldosterone
Polycystic ovary syndrome
  • Polycystic ovaries in sonography
  • Obesity
  • PCOS is the most common cause of hirsutism in women
  • No evidence another diagnosis
Adrenal tumors
  • Older age
  • Rapidly progressive symptoms
Ovarian virilizing tumor
  • Older age
  • Rapidly progressive symptoms
Cushing's syndrome.
hyperprolactinemia
Ovarian hyperthecosis 
Syndromes of severe insulin resistance

References