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COMMON MUTATIONS MTDNA PANEL, EDTA BLOOD

This panel detects common mitochondrial DNA mutations associated with disorders like MELAS, MERRF, NARP, LHON, and KSS. It helps diagnose mitochondrial diseases, which can cause neurological and muscular symptoms. Early diagnosis allows for better management of these genetic conditions.

Also known asCommon Mutation Panel Mtdna (melas 1MerrfNarpLhon

Available via

Home Collection, Lab Visit

Contains

5 parameters

Earliest reports in

8 Working Days

Test details

COMMON MUTATIONS MTDNA PANEL, EDTA BLOOD Test in Bengaluru Overview

Preparations

No special preparations needed

Test included
COMMON MUTATIONS MTDNA PANEL, EDTA BLOOD includes 5 parameters

  • Melas
  • Merrf
  • Narp
  • Lhon
  • Kearns–sayre Syndrome (kss) Mtdna Mutation
Frequently Asked Questions

This genetic screening test detects common gene mutations linked to inherited diseases or cancer susceptibility.

Individuals with a family history of genetic disorders, cancer risk, or unexplained symptoms related to hereditary conditions should take this test.

A blood or saliva sample is analyzed for specific gene mutations.

A positive result suggests a genetic predisposition to certain diseases, requiring further medical evaluation.

While mutations cannot be reversed, early detection can help manage risks through lifestyle changes and medical interventions.

Test code

RD1465

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 - 10:00

Turn around time

8 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

COMMON MUTATIONS MTDNA PANEL, EDTA BLOOD

₹13000