Congenital adrenal hyperplasia laboratory tests: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | |||
Please help WikiDoc by adding more content here. It's easy! Click [[Help:How_to_Edit_a_Page|here]] to learn about editing. | |||
{{Congenital adrenal hyperplasia}} | {{Congenital adrenal hyperplasia}} | ||
| Line 4: | Line 7: | ||
==Overview== | ==Overview== | ||
==Laboratory Findings== | ==Laboratory Findings== | ||
Revision as of 18:05, 22 August 2012
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
|
Congenital adrenal hyperplasia main page |
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.