Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
Deafness (Cx 26) Mutation
7,770 THB
SKU :
MD-NLB400
Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness.
Lab Categories : Children, Congenital Deafness, EDTA Whole Blood, Genetic Disorder, Hearing Loss, Infants, Lab Test, PCR + DNA Sequencing
Diseases : Congenital Deafness
Symptoms : Hearing Loss
Habits : Genetic Disorder
Specimens : EDTA Whole Blood
Diagnostic Methods : DNA Sequencing, PCR
| Also Known As | Cx26 Genetic Deafness Test |
|---|---|
| Specimen | EDTA whole blood 6-10 ml (minimum 5 ml) |
| Turnaround Time | 1 month |
| Test Code | MD-NLB400 |
| Test Type | Special |
| Related Tests | Genetic Hearing Loss Panel |
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