17 alpha-hydroxylase deficiency (patient information)
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency |
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Template:WikiDoc Sources
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
For the WikiDoc page for this topic, click here.
Overview
What are the symptoms of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency?
What causes congenital adrenal hyperplasia due to 11β-hydroxylase deficiency?
Who is at highest risk?
Diagnosis
When to seek urgent medical care?
Treatment options
Where to find medical care for congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency?
Prevention
What to expect (Outlook/Prognosis)?
The prognosis of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency is generally good with treatment.[1]
Possible complications
Reference
- ↑ https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency URL Accessed on 10/15/2015