17 alpha-hydroxylase deficiency laboratory findings: Difference between revisions
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==Laboratory Findings== | ==Laboratory Findings== | ||
* Elevated levels of 11-deoxycorticosterone | * Elevated levels of 11-deoxycorticosterone | ||
* Elevated levels of corticosterone | * Elevated levels of [[corticosterone]] | ||
* Elevated adrenocorticotropic hormone | * Elevated [[adrenocorticotropic hormone]] | ||
* Elevated follicle-stimulating hormone | * Elevated [[follicle-stimulating hormone]] | ||
* Elevated luteinizing hormone | * Elevated [[luteinizing hormone]] | ||
* Decreased serum levels of 17-hydroxypregnenolone<ref name="AlqahtaniShati2015">{{cite journal|last1=Alqahtani|first1=Mohammad A.|last2=Shati|first2=Ayed A.|last3=Zou|first3=Minjing|last4=Alsuheel|first4=Ali M.|last5=Alhayani|first5=Abdullah A.|last6=Al-Qahtani|first6=Saleh M.|last7=Gilban|first7=Hessa M.|last8=Meyer|first8=Brain F.|last9=Shi|first9=Yufei|title=A Novel Mutation in theCYP11B1Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy|journal=International Journal of Endocrinology|volume=2015|year=2015|pages=1–5|issn=1687-8337|doi=10.1155/2015/595164}}</ref> | * Decreased serum levels of 17-hydroxypregnenolone<ref name="AlqahtaniShati2015">{{cite journal|last1=Alqahtani|first1=Mohammad A.|last2=Shati|first2=Ayed A.|last3=Zou|first3=Minjing|last4=Alsuheel|first4=Ali M.|last5=Alhayani|first5=Abdullah A.|last6=Al-Qahtani|first6=Saleh M.|last7=Gilban|first7=Hessa M.|last8=Meyer|first8=Brain F.|last9=Shi|first9=Yufei|title=A Novel Mutation in theCYP11B1Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy|journal=International Journal of Endocrinology|volume=2015|year=2015|pages=1–5|issn=1687-8337|doi=10.1155/2015/595164}}</ref> | ||
* Decreased 17-hydroxyprogesterone | * Decreased 17-hydroxyprogesterone | ||
* Decreased 11-deoxycortisol | * Decreased 11-deoxycortisol | ||
* Decreased cortisol | * Decreased [[cortisol]] | ||
* Decreased dehydroepiandrosterone | * Decreased [[dehydroepiandrosterone]] | ||
* Decreased | * Decreased [[androstenedione]] | ||
* Decreased | * Decreased [[testosterone]] | ||
* Decreased 17-hydroxylase corticosteroid | * Decreased 17-hydroxylase corticosteroid | ||
* Decreased urinary 17-ketosteroid | * Decreased urinary 17-ketosteroid | ||
* Decreased | * Decreased [[estrogen]] | ||
* Decreased | * Decreased [[aldosterone]] | ||
* Decreased | * Decreased [[renin]] | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} |
Revision as of 15:37, 9 February 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
Laboratory findings consistent with the diagnosis of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency include elevated 17α-hydroxyprogesterone, elevated androstenedione, elevated urinary 17-ketosteroids and decreased renin.
Laboratory Findings
- Elevated levels of 11-deoxycorticosterone
- Elevated levels of corticosterone
- Elevated adrenocorticotropic hormone
- Elevated follicle-stimulating hormone
- Elevated luteinizing hormone
- Decreased serum levels of 17-hydroxypregnenolone[1]
- Decreased 17-hydroxyprogesterone
- Decreased 11-deoxycortisol
- Decreased cortisol
- Decreased dehydroepiandrosterone
- Decreased androstenedione
- Decreased testosterone
- Decreased 17-hydroxylase corticosteroid
- Decreased urinary 17-ketosteroid
- Decreased estrogen
- Decreased aldosterone
- Decreased renin
References
- ↑ Alqahtani, Mohammad A.; Shati, Ayed A.; Zou, Minjing; Alsuheel, Ali M.; Alhayani, Abdullah A.; Al-Qahtani, Saleh M.; Gilban, Hessa M.; Meyer, Brain F.; Shi, Yufei (2015). "A Novel Mutation in theCYP11B1Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy". International Journal of Endocrinology. 2015: 1–5. doi:10.1155/2015/595164. ISSN 1687-8337.