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Pendred syndrome (SLC26A4) (Genome star)
SKU: MD-NLMM524 Categories: , , , , , , , Tags: , , , , ,

In Stock

Pendred syndrome (SLC26A4) (Genome star)

฿107,100.00

Additional information

Also Known As

SLC26A4 Gene Test, Pendred Syndrome Test
Specimen

EDTA blood 6 ml
Turnaround Time

1 month
Test Code

MD-NLMM524
Test Type

Special
Related Tests

Genetic Screening Panel, Exome Sequencing

Detects mutations in the SLC26A4 gene associated with Pendred syndrome, a genetic disorder leading to hearing loss and thyroid dysfunction.

Product tags: Genetic Disorders, Hearing Loss, None, Pendred Syndrome Test, SLC26A4 Gene Test, Thyroid Issues
Diseases: Genetic Disorders, Hearing Loss
Symptoms: Hearing Loss, Thyroid Issues
Habits: None
Age Groups: All Ages
Specimens: EDTA Whole Blood
Diagnostic Methods: Next-Generation Sequencing (NGS)
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Description

Detects mutations in the SLC26A4 gene associated with Pendred syndrome, a genetic disorder leading to hearing loss and thyroid dysfunction.

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

SLC26A4 Gene Test, Pendred Syndrome Test
Specimen

EDTA blood 6 ml
Turnaround Time

1 month
Test Code

MD-NLMM524
Test Type

Special
Related Tests

Genetic Screening Panel, Exome Sequencing

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