Congenital Adrenal Hyperplasia (CAH) Profile for 21-Hydroxylase Deficiency
NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.
Preferred screening test for congenital adrenal hyperplasia (CAH) that is caused by 21-hydroxylase deficiency
Part of a battery of tests to evaluate females with hirsutism or infertility, which can result from adult-onset CAH
Genetics Test Information Provides information that may help with selection of the correct test or proper submission of the test request
Preferred screening test for congenital adrenal hyperplasia (CAH) that is caused by 21-hydroxylase deficiency. Also useful as part of a battery of tests to evaluate females with hirsutism or infertility, which can result from adult-onset CAH.
Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.
|Test ID||Reporting Name||Available Separately||Always Performed|
|CORTI||Cortisol, S||Yes, (order CINP)||Yes|
|ANDRO||Androstenedione, S||Yes, (order ANST)||Yes|
|H17||17-Hydroxyprogesterone, S||Yes, (order OHPG)||Yes|
Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name
21 Hydroxylase Deficiency
CAH (Congenital Adrenal hyperplasia)
17-Alpha Hydroxyprogesterone (17-OHP)
Progesterone, 17-Alpha Hydroxy