GORDON HOLMES SYNDROME (RNF216 AND OTUD4) GENE

Gordon Holmes syndrome is a rare subtype of chronic cerebellar ataxia, infrequently reported in literature. The syndrome should be considered if chronic ataxia is associated with reproductive abnormalities. The meticulous clinical approach for chronic ataxia is required to pinpoint precise diagnosis

Also known asGordon Holmes Syndrome (rnf216 And Otud4) Gene Sequencing Gordon Holmes Syndrome (rnf216 And Otud4) Gene Sequencing

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
GORDON HOLMES SYNDROME (RNF216 AND OTUD4) GENE includes 1 parameter

  • Specimen

Test code

G696

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

GORDON HOLMES SYNDROME (RNF216 AND OTUD4) GENE

22000