UREA CYCLE DEFECTS GENE PANEL

A panel of genetic tests used to identify mutations in genes involved in the urea cycle, a process that detoxifies ammonia in the liver. Defects in this cycle can cause hyperammonemia and neurological issues, such as in Ornithine Transcarbamylase deficiency.

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
UREA CYCLE DEFECTS GENE PANEL includes 1 parameter

  • Specimen

Test code

G682

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

UREA CYCLE DEFECTS GENE PANEL

22000