CONNEXIN 26 GENE MUTATION, EDTA BLOOD
Detects mutations in the connexin 26 gene, a common cause of hereditary hearing loss. It is used for diagnosing genetic hearing impairment in infants and children.
Also known asConnexin 26 Mutation Connexin 26 Mutation
Test details
Preparations
No special preparations needed
Test included
CONNEXIN 26 GENE MUTATION, EDTA BLOOD includes 2 parameters
- Preliminary Report
- Connexin Gene Mutation Test - Non-syndromic Hearing Loss
Test code
RD1309
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 5 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
CONNEXIN 26 GENE MUTATION, EDTA BLOOD
Package price
₹6000
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₹6000