21-hydroxylase deficiency differential diagnosis: Difference between revisions
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==Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases== | ==Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases== | ||
[[Congenital adrenal hyperplasia]] due to 21-hydroxylase deficiency must be differentiated from diseases that cause [[ambiguous genitalia]] | [[Congenital adrenal hyperplasia]] due to 21-hydroxylase deficiency classic type must be differentiated from diseases that cause [[ambiguous genitalia]]: | ||
{| class="wikitable" | {| class="wikitable" | ||
!Disease name | !Disease name | ||
! | !Elevated | ||
! | Steroids | ||
! | !Decreased steroids | ||
!Androgen status | |||
!Important distinguishing findings | |||
|- | |- | ||
|[[ | |Classic type of 21-hydroxylase deficiency | ||
|17-OHP | |||
Progesterone | |||
Androstenedione | |||
DHEA | |||
|Aldosterone | |||
Corticosterone (salt-wasting) | |||
Cortisol (simple virilizing) | |||
| | |||
|- | |||
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | |||
|DOC | |||
11-Deoxy- | |||
cortisol | |||
|Cortisol | |||
Corticosterone | |||
Aldosterone | |||
| | |||
|- | |||
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | |||
|DOC | |||
Corticosterone | |||
Progesterone | |||
|Cortisol | |||
Aldosterone | |||
| | |||
|- | |||
|3β-Hydroxysteroid Dehydrogenase | |||
|DHEA | |||
17-OH pregneno-lone | |||
Pregnenolone | |||
|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: | |||
{| class="wikitable" | |||
!Disease name | |||
!Elevated | |||
Steroids | |||
!Decreased steroids | |||
!Androgen status | |||
!Important distinguishing findings | |||
|- | |||
|Non-classic type of 21-hydroxylase deficiency | |||
|17-OHP | |||
Exaggerated androstene-dione, DHEA, and 17-OHP | |||
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 | |||
11-Deoxy- | |||
cortisol | |||
|Cortisol | |||
Corticosterone | |||
Aldosterone | |||
| | |||
|- | |||
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | |||
|DOC | |||
Corticosterone | |||
Progesterone | |||
|Cortisol | |||
Aldosterone | |||
| | |||
|- | |||
|3β-Hydroxysteroid Dehydrogenase | |||
|DHEA | |||
17-OH pregneno-lone | |||
Pregnenolone | |||
|Cortisol | |||
Aldosterone | |||
| | |||
|- | |||
|Polycystic ovary syndrome | |||
| | |||
| | |||
| | |||
| | |||
* Polycystic ovaries in sonography | |||
* Obesity | |||
|- | |||
|Adrenal tumors | |||
| | |||
| | |||
| | |||
|- | |||
|Ovarian virilizing tumor | |||
| | |||
| | |||
| | |||
|- | |||
|Cushing's syndrome. | |||
| | | | ||
| | | | ||
| | | | ||
|- | |- | ||
| | |hyperprolactinemia | ||
| | | | ||
| | | | ||
| | | | ||
|- | |- | ||
| | |Ovarian hyperthecosis | ||
| | | | ||
| | | | ||
| | | | ||
|- | |- | ||
| | |Syndromes of severe insulin resistance | ||
| | | | ||
| | | | ||
| | | | ||
|} | |} | ||
== References == | == References == |
Revision as of 19:13, 14 July 2017
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters |
Differentiating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
21-hydroxylase deficiency differential diagnosis On the Web |
American Roentgen Ray Society Images of 21-hydroxylase deficiency differential diagnosis |
21-hydroxylase deficiency differential diagnosis in the news |
Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
Risk calculators and risk factors for 21-hydroxylase deficiency differential diagnosis |
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 | Elevated
Steroids |
Decreased steroids | Androgen status | Important distinguishing findings |
---|---|---|---|---|
Classic type of 21-hydroxylase deficiency | 17-OHP
Progesterone Androstenedione DHEA |
Aldosterone
Corticosterone (salt-wasting) Cortisol (simple virilizing) |
||
11-β hydroxylase deficiency | DOC
11-Deoxy- cortisol |
Cortisol
Corticosterone Aldosterone |
||
17-α hydroxylase deficiency | DOC
Corticosterone Progesterone |
Cortisol
Aldosterone |
||
3β-Hydroxysteroid Dehydrogenase | DHEA
17-OH pregneno-lone Pregnenolone |
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 | 17-OHP
Exaggerated androstene-dione, DHEA, and 17-OHP response to ACTH |
None | ||
11-β hydroxylase deficiency | DOC
11-Deoxy- cortisol |
Cortisol
Corticosterone Aldosterone |
||
17-α hydroxylase deficiency | DOC
Corticosterone Progesterone |
Cortisol
Aldosterone |
||
3β-Hydroxysteroid Dehydrogenase | DHEA
17-OH pregneno-lone Pregnenolone |
Cortisol
Aldosterone |
||
Polycystic ovary syndrome |
| |||
Adrenal tumors | ||||
Ovarian virilizing tumor | ||||
Cushing's syndrome. | ||||
hyperprolactinemia | ||||
Ovarian hyperthecosis | ||||
Syndromes of severe insulin resistance |