LEIGH SYNDROME & MITOCHONDRIAL ENCEPHALOPATHY GENE
This gene panel tests for mutations associated with Leigh syndrome, a severe neurological disorder. It helps diagnose mitochondrial encephalopathy and provides insights into genetic causes of progressive neurological decline.
Also known asLeigh Syndrome & Mitochondrial Encephalopathy Gene Panel Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel
Test details
Preparations
No special preparations needed
Test included
LEIGH SYNDROME & MITOCHONDRIAL ENCEPHALOPATHY GENE includes 1 parameter
- Leigh Syndrome & Mitochondrial Encephalopathy
Test code
G534
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Amniotic Fluid | Plain Sterile Vaccutainer | 3 ML |
| Peripheral Blood | Others | 3 ML |
Specimen stability information
Amniotic Fluid, Peripheral Blood
Collection instructions
Age,Gender,Clinical history required
Specimen rejection criteria
Test run frequency
Every Day TIME - 08:00
Turn around time
28 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
LEIGH SYNDROME & MITOCHONDRIAL ENCEPHALOPATHY GENE
Package price
₹22000
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₹22000