SPINAL MUSCULAR ATROPHY MICRODELETION PCR

A genetic test that detects microdeletions in the SMN1 gene, which causes spinal muscular atrophy (SMA), a genetic disorder that affects motor neurons and causes muscle weakness.

Also known asSpinal Muscular Atrophy Microdeletion Pcr Spinal Muscular Atrophy Microdeletion Pcr

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

8 Working Days

Test details

SPINAL MUSCULAR ATROPHY MICRODELETION PCR Test in Mangaluru Overview

Preparations

No special preparations needed

Test included
SPINAL MUSCULAR ATROPHY MICRODELETION PCR includes 1 parameter

  • Spinal Muscular Atrophy Microdeletion Pcr
Frequently Asked Questions

This test detects microdeletions in the SMN1 gene, which cause spinal muscular atrophy (SMA), a genetic neuromuscular disorder.

This test is recommended for:

  • Pregnant women with a family history of SMA.
  • Couples undergoing carrier screening.
  • Individuals with suspected SMA.

A sample (amniotic fluid, blood, or tissue) is analyzed using PCR techniques.

  • Positive for Microdeletion: Confirms SMA diagnosis.
  • Negative Result: No microdeletion detected.

Early detection allows informed decisions and early intervention for SMA.

Test code

8764

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Edta Whole BloodLavender Vacutainer3 ML

Specimen stability information

Edta Whole Blood

Collection instructions

Clinical History

Specimen rejection criteria

Test run frequency

Every Day TIME - 09:30

Turn around time

8 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

SPINAL MUSCULAR ATROPHY MICRODELETION PCR

3100