Congenital adrenal hyperplasia laboratory tests

Revision as of 13:30, 20 September 2012 by Daniel Nethala (talk | contribs)
Jump to navigation Jump to search

Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.

Congenital adrenal hyperplasia main page

Overview

Classification

21-hydroxylase deficiency
11β-hydroxylase deficiency
17 alpha-hydroxylase deficiency
3 beta-hydroxysteroid dehydrogenase deficiency
Cytochrome P450-oxidoreductase (POR) deficiency (ORD)
Lipoid congenital adrenal hyperplasia

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

Laboratory Findings

Electrolyte and Biomarker Studies

In 11-hydroxylase deficiencis, hypokalemia is present in 2/3 and help distinguish from 21-hydroxylase deficiencies.

References


Template:WikiDoc Sources