11β-hydroxylase deficiency differential diagnosis
11β-hydroxylase deficiency Microchapters |
Differentiating 11β-hydroxylase deficiency from other Diseases |
Diagnosis |
Treatment |
Case Studies |
11β-hydroxylase deficiency differential diagnosis On the Web |
American Roentgen Ray Society Images of 11β-hydroxylase deficiency differential diagnosis |
11β-hydroxylase deficiency differential diagnosis in the news |
Directions to Hospitals Treating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency |
Risk calculators and risk factors for 11β-hydroxylase deficiency differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]
21-hydroxylase deficiency Microchapters |
Differentiating 21-Hydroxylase Deficiency from other Diseases |
Diagnosis |
Treatment |
Case Studies |
11β-hydroxylase deficiency differential diagnosis On the Web |
American Roentgen Ray Society Images of 11β-hydroxylase deficiency differential diagnosis |
11β-hydroxylase deficiency differential diagnosis in the news |
Risk calculators and risk factors for 11β-hydroxylase deficiency differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3] Mehrian Jafarizade, M.D [4]
Overview
11β-hydroxylase deficiencymust be differentiated from 21-hydroxylase deficiency, 17 alpha-hydroxylase deficiency, androgen insensitivity syndrome, polycystic ovarian syndrome, and adrenal tumor.
Differentiating 11β-hydroxylase deficiency from other diseases
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency classic type must be differentiated from diseases that cause ambiguous genitalia:[1][2]
Disease name | Steroid status | Other laboratory | Important clinical findings |
---|---|---|---|
Classic type of 21-hydroxylase deficiency | Increased:
Decreased:
|
|
|
11-β hydroxylase deficiency | Increased:
Decreased:
|
|
|
17-α hydroxylase deficiency | Increased:
Decreased:
|
Low testosterone levels |
|
3β-Hydroxysteroid Dehydrogenase | Increased:
Decreased:
|
|
|
Gestational hyperandrogenism |
|
|
|
References
- ↑ Hughes IA, Nihoul-Fékété C, Thomas B, Cohen-Kettenis PT (2007). "Consequences of the ESPE/LWPES guidelines for diagnosis and treatment of disorders of sex development". Best Pract. Res. Clin. Endocrinol. Metab. 21 (3): 351–65. doi:10.1016/j.beem.2007.06.003. PMID 17875484.
- ↑ White PC, Speiser PW (2000). "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency". Endocr. Rev. 21 (3): 245–91. doi:10.1210/edrv.21.3.0398. PMID 10857554.