Pendred Syndrome by SLC26A4 Gene Sequencing*

Sequences the SLC26A4 gene to identify variants associated with Pendred syndrome and SLC26A4-related hearing loss.

฿22,190.00

Sequences the SLC26A4 gene to identify variants associated with Pendred syndrome and SLC26A4-related hearing loss.

Blood

15 min at lab

Results: 30 days

Typical Use

Used to investigate suspected inherited sensorineural hearing loss, particularly with an enlarged vestibular aqueduct, thyroid involvement or a relevant family history.

Preparation

Wear clothing that allows easy access to your arm

Arrive well-hydrated

Continue regular medications unless advised otherwise by your doctor

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