Common Mutations mtDNA Panel
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.
Common Mutations mtDNA Panel Test in Panchkula Overview
No special preparations needed
- Melas
- Merrf
- Narp
- Lhon
- Kearns–sayre Syndrome (kss) Mtdna Mutation
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
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 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
Package price
₹13000
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₹13000