RETT SYNDROME DELETION & DUPLICATION DETECTION

This test detects deletions and duplications in the MECP2 gene, which are responsible for Rett syndrome, a neurodevelopmental disorder. It aids in diagnosing and confirming Rett syndrome.

Also known asRett Syndrome Deletion & Duplication Detection Rett Syndrome Deletion & Duplication Detection

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

12 Working Days

Test details
Preparations

No special preparations needed

Test included
RETT SYNDROME DELETION & DUPLICATION DETECTION includes 1 parameter

  • Rett Syndrome Deletion & Duplication Detection

Test code

G552

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Peripheral BloodOthers3 ML

Specimen stability information

Peripheral Blood

Specimen rejection criteria

Test run frequency

Every Day TIME - 08:00

Turn around time

12 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

RETT SYNDROME DELETION & DUPLICATION DETECTION

7000