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.

Also known asPrimary Hyperoxaluria Gene Panel Primary Hyperoxaluria Gene Panel

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