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Test ID: FSTS    
Steroid Sulfatase Deficiency, Xp22.3 Deletion, FISH

Available on the App Store

Secondary ID A test code used for billing and in test definitions created prior to November 2011

88539

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Useful For Suggests clinical disorders or settings where the test may be helpful

As an aid in the diagnosis of steroid sulfatase deficiency syndrome, in conjunction with CMS / Chromosomes Analysis, for Congenital Disorders, Blood

 

Detecting cryptic translocations involving Xp22.3 that are not demonstrated by conventional chromosome studies

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

Fluorescence In Situ Hybridization (FISH)

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

STS, Xp22.3, FISH

Aliases Lists additional common names for a test, as an aid in searching

FISH
Steroid Sulfatase Deficiency
STS
X Linked Icthiosis
X Linked Icthyosis
Xp Deletion
Xp22.3