Congenital adrenal hyperplasia laboratory tests: Difference between revisions

Jump to navigation Jump to search
(Created page with "{{Congenital adrenal hyperplasia}} {{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} ==Overview== ==Laboratory Findings== ==== Electrolyte and Biomarker Studies ==== In 11...")
 
No edit summary
Line 4: Line 4:


==Overview==
==Overview==
Please help WikiDoc by adding more content here.  It's easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.


==Laboratory Findings==
==Laboratory Findings==
Line 13: Line 15:
{{Reflist|2}}
{{Reflist|2}}


[[Category:Disease]]
[[Category:Needs content]]
[[Category:Pediatrics]]
[[Category:Endocrinology]]
[[Category:Genetic disorders]]


{{WikiDoc Help Menu}}
{{WikiDoc Help Menu}}
{{WikiDoc Sources}}
{{WikiDoc Sources}}

Revision as of 05:14, 22 August 2012

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

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


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