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Deafness (Cx 26) Mutation
SKU: MD-NLB400 Categories: , , , , , , , Tags: , , ,

In Stock

Deafness (Cx 26) Mutation

฿7,770.00

Additional information

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

Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness.

Product tags: Congenital Deafness, Cx26 Genetic Deafness Test, Genetic Disorder, Hearing Loss
Diseases: Congenital Deafness
Symptoms: Hearing Loss
Habits: Genetic Disorder
Age Groups: Children, Infants
Specimens: EDTA Whole Blood
Diagnostic Methods: DNA Sequencing, PCR
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Description

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.

Additional information

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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