Test Catalog

Test ID: MPS2Z    
Hunter Syndrome, Full Gene Analysis, Varies

Method Description Describes how the test is performed and provides a method-specific reference

Bidirectional sequence analysis is performed to test for the presence of a variant in all coding regions and intron/exon boundaries of the IDS gene.(Unpublished Mayo method)


In addition, a PCR-based assay is utilized to examine DNA for the presence of rearrangements between the IDS gene and pseudogene, IDSP1.(Lagerstedt K, Karsten SL, Carlberg BM, et al: Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome. Hum Mol Genet. 1997;6[4]:627-633)

PDF Report Indicates whether the report includes an additional document with charts, images or other enriched information


Day(s) Performed Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.


Report Available The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

14 to 20 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

Whole Blood: 2 weeks (if available); Extracted DNA: 3 months

Performing Laboratory Location Indicates the location of the laboratory that performs the test