PRIMARY HYPEROXALURIA GENE PANEL

A genetic test that identifies mutations in the genes responsible for primary hyperoxaluria, a rare metabolic disorder causing excessive oxalate production, leading to kidney stones and renal failure.

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
PRIMARY HYPEROXALURIA GENE PANEL includes 1 parameter

  • Results

Test code

MGEN008

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Edta Whole BloodLavender Vacutainer

Specimen stability information

Edta Whole Blood

Specimen rejection criteria

Test run frequency

Monday,Tuesday,Wednesday,Thursday TIME - 09:30

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

PRIMARY HYPEROXALURIA GENE PANEL

19000