Test ID: FSTS
Steroid Sulfatase Deficiency, Xp22.3 Deletion, FISH
Method Description
Describes how the test is performed and provides a method-specific reference
Identification of the steroid sulfatase deficiency deletion is based on FISH analysis of the critical region (STS) on the short arm of the X chromosome (Xp22.3). Metaphase cells are examined for the presence of critical region loci at Xp22.3 (orange signal) and the control probe at the X centromere (green signal). In metaphase cells with a deletion, the abnormal (deleted) X chromosome will exhibit only a control probe signal, while signals for both the critical region and the control probes will be present on the normal X chromosome. (Crifase PA, Michels VV, Driscoll DJ, et al: DNA fluorescent probes for diagnosis of velocardio-facial and related syndromes. Mayo Clin Proc 1995;195[70]:1148-1153)
Day(s) and Time(s) Test Performed
Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.
Samples processed Monday through Sunday. Results reported Monday through Friday, 8 a.m.-5 p.m. CST.


