Test ID: FSTS
Steroid Sulfatase Deficiency, Xp22.3 Deletion, FISH
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/8696 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
Steroid Sulfatase Deficiency
STS
X Linked Icthiosis
X Linked Icthyosis
Xp Deletion
Xp22.3
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