Page 385 - SRL Diagnostics Directory of Servies
P. 385

SR #      TEST NAME                              TAT

                       190     Spastic Paraplegia NGS Panel 58 genes  8 WEEKS
                       191     Squamous Cell Carcinoma Ag             7 - 10 DAYS
                       192     Steroid-Resistant Nephrotic Syndrome 14-gene   6 - 8 WEEKS
                               panel
                       193     Steroid-Resistant Nephrotic Syndrome 14-gene   6 - 8 WEEKS
                               panel (ACTN4, CD2AP, COQ2, INF2, LAMB2,
                               LMX1B, NPHS1, NPHS2, PDSS2, PLCE1,
                               SCARB2, SMARCAL1, TRPC6, WT1)
                       194     Strontium, Blood                       10 DAYS
                       195     Strontium, Serum/Plasma                10 DAYS
                       196     Strontium, Urine                       10 DAYS
                       197     Substance P                            7 - 10 DAYS
                       198     SUCLA2 Gene                            8 WEEKS
                       199     Superoxide dismutase (SOD)             10 DAYS
                       200     TCN2 gene associated with Transcobalamin II   8 WEEKS
                               Deficiency
                       201     Testosterone, Saliva                   2 WEEKS
                       202     Titin Abs                              7 - 10 DAYS
                       203     Tocopherol (Vitamin E)                 5 - 7 DAYS
                       204     TRAPS                                  6 WEEKS
                       205     Tropheryma whipplei PCR                7 - 10 DAYS
                       206     Type 1 Neurofibromatosis testing involves full   8 WEEKS
                               sequencing + deletion/duplication testing for the
                               NF1 + SPRED1 genes
                       207     Type 2 (NF2-related) Neurofibromatosis is less   8 WEEKS
                               common and usually has bilateral vestibular
                               schwannomas and acoustic involvement
                               (impaired hearing).  Sequencing + deletion/du-
                               plication testing for the NF2 gene
                       208     UROD Gene                              4 - 6 WEEKS
                       209     Vitamin C/ Ascorbic Acid               7 - 10 DAYS
                       210     Voltage-Gated Potassium Channel (VGKC)   15 DAYS
                               Antibody
                       211     Whole exome sequencing (80-100x), Offered as   12 WEEKS
                               a family trio (one price, three samples – to
                               include affected child + parents.  Additional
                               affected children can be added for free).
                       212     Whole Genome Sequencing                12 WEEKS
                       213     William syndrome                       7 - 10 DAYS
                       214     Zinc-Protoporphyrin in RBC (HPLC)      5 - 7 DAYS
                       215                                            10 DAYS
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