11β-hydroxylase deficiency laboratory findings: Difference between revisions
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(Created page with "__NOTOC__ {{}} {{CMG}}; {{AE}} {{Ammu}} ==Overview== ==Laboratory Findings== * Elevated serum levels of DOC * Elevated 17-OHP * Elevated androstenedione * Decreased cortisol...") |
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{{}} | {{Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency}} | ||
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==Overview== | ==Overview== |
Revision as of 17:01, 26 January 2016
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases |
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Diagnosis |
Treatment |
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11β-hydroxylase deficiency laboratory findings On the Web |
American Roentgen Ray Society Images of 11β-hydroxylase deficiency laboratory findings |
Directions to Hospitals Treating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency |
Risk calculators and risk factors for 11β-hydroxylase deficiency laboratory findings |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Laboratory Findings
- Elevated serum levels of DOC
- Elevated 17-OHP
- Elevated androstenedione
- Decreased cortisol
- Decreased Aldosterone
References