HEREDITARY SPASTIC PARAPLEGIA

This test looks for genetic mutations responsible for hereditary spastic paraplegia, a neurological disorder characterized by progressive stiffness and weakness in the lower limbs. Early identification helps in symptomatic treatment and genetic counseling. The condition is typically inherited in an autosomal dominant or recessive manner.

Also known asHereditary Spastic Paraplegia Hereditary Spastic Paraplegia

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
HEREDITARY SPASTIC PARAPLEGIA includes 1 parameter

  • Results

Test code

MGEN005

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer
Edta Whole BloodLavender Vacutainer
Others (fx)Others

Specimen stability information

Amniotic Fluid, Edta Whole Blood, Others (Fx)

Collection instructions

Age,Gender,Clinical history required

Specimen rejection criteria

Test run frequency

Monday,Tuesday,Wednesday,Thursday TIME - 09:30

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

HEREDITARY SPASTIC PARAPLEGIA

19000