Pontocerebellar hypoplasia gene panel

A genetic test to identify mutations causing pontocerebellar hypoplasia, a rare neurodegenerative disorder affecting the brain's cerebellum and pons. It helps in the diagnosis of this condition.

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
Pontocerebellar hypoplasia gene panel includes 1 parameter

  • Specimen

Test code

G778

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

Pontocerebellar hypoplasia gene panel

22000