MCARDLE DISEASE (PYGM) GENE ANALYSIS

A genetic test that analyzes mutations in the PYGM gene, which encodes the enzyme responsible for breaking down glycogen in muscles. This test helps diagnose McArdle disease, a metabolic disorder affecting muscle function.

Also known asMcardle Disease (pygm) Gene Analysis Mcardle Disease (pygm) Gene Analysis

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
MCARDLE DISEASE (PYGM) GENE ANALYSIS includes 1 parameter

  • Specimen

Test code

G665

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

MCARDLE DISEASE (PYGM) GENE ANALYSIS

22000