Foresight TM Carrier Scr with FRX (UCSFRX) Build info

Synonyms

• FORESIGHT TM CARRIER SCR WITH FRX (UCSFRX)
• LAB11538

Procedure Name

FORESIGHT TM CARRIER SCR WITH FRX (UCSFRX)

Procedure Master Number

LAB11538

Procedure ID

115391

Clinical Info

The test can detect over 176 health conditions that can be passed unknowingly from parent to child plus Fragile X. Some of the conditions on the Family Prep Screen can be treated early in life, like Wilson disease and PKU. Some result in intellectual disabilities, as with fragile X syndrome and Niemann-Pick disease. Others are chronic and require lifelong management, like Cystic Fibrosis and Bloom syndrome. Finally, some of the conditions have no treatments available, like spinal muscular atrophy and Canavan disease.

Specimen Sources

Specimen Types

Container

Collection Instructions

Container/Tube:  Lavender top tube(s)
Specimen: Whole Blood 3 ml's
Transport Temperature: Room Temperature
 
Note:
Requires Ethnicity (required for interpretation)
 Choices are:
Northern European (British, German) Southern European (Italian, Greek) French Canadian Ashkenazi Jewish Finnish Other/Mixed Caucasian East Asian (Chinese, Japanese) South Asian (Indian, Pakistani) Southeast Asian (Filipino, Vietnamese) African or African American Hispanic Middle Eastern Native American Pacific Islander Unknown

Specimen Volume

Whole Blood 3 ml's

Transport Instructions

Room Temperature

Specimen Stability

Methodology

Next-generation Sequencing
 
Turnaround time: 2 weeks

Days Performed

Performing Laboratory

Myriad Genetics

CPT

81200                 
81205
81209
81220
81242
81250
81251
81255
81260
81290
81330
81332
81243

PDM

Only Orderable at Locations:

Results

Result Interpretation

See Report

Forms