DRAVET SYNDROME (SCN1A) GENE ANALYSIS

A genetic test to identify mutations in the SCN1A gene, which causes Dravet syndrome, a severe form of epilepsy in infants.

Also known asDravet Syndrome (scn1a) Gene Analysis Dravet Syndrome (scn1a) 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
DRAVET SYNDROME (SCN1A) GENE ANALYSIS includes 1 parameter

  • Specimen

Test code

G674

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

DRAVET SYNDROME (SCN1A) GENE ANALYSIS

22000