WAARDENBURG SYNDROME GENE PANEL

A genetic test to identify mutations in several genes (such as PAX3 and MITF) associated with Waardenburg syndrome, a genetic condition that causes hearing loss, pigmentary changes in the hair and skin, and sometimes vision problems.

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
WAARDENBURG SYNDROME GENE PANEL includes 1 parameter

  • Specimen

Test code

G650

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Others (fx)Others2 ML

Specimen stability information

Others (Fx)

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

WAARDENBURG SYNDROME GENE PANEL

22000