BARTTER SYNDROME GENE PANEL

A genetic test that identifies mutations associated with Bartter syndrome, a rare kidney disorder that causes an imbalance in electrolytes. It is used to diagnose and confirm the condition.

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
BARTTER SYNDROME GENE PANEL includes 1 parameter

  • Specimen

Test code

G678

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

BARTTER SYNDROME GENE PANEL

22000