MONDINI DEFECT (SLC26A4) GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited    
The Mondini Defect (SLC26A4) Gene Panel by NGS is a comprehensive genetic test designed to detect mutations in the SLC26A4 gene associated with Mondini dysplasia, a congenital inner ear malformation leading to hearing loss. This test helps identify underlying genetic causes, enabling early diagnosis and improved clinical management. Performed on EDTA blood, the panel uses advanced Next Generation Sequencing technology for accurate mutation profiling. Metropolis Healthcare offers high-quality molecular testing support to guide treatment planning and family genetic counseling

  • 17 Crores+ Samples Processed
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Price: Rs. 19,950.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0128

Frequently Asked Questions (FAQ's):

What is Mondini Defect?
It is a congenital malformation of the inner ear structure that can cause sensorineural hearing loss or hearing impairment.

Why is the SLC26A4 gene tested?
Mutations in the SLC26A4 gene are commonly linked to Mondini dysplasia and Pendred syndrome, helping clarify the genetic basis of hearing loss.

How is this test performed?
The analysis is done using Next Generation Sequencing (NGS) technology at Metropolis Healthcare for high accuracy and detailed results.

What sample is required?
EDTA whole blood sample is required for testing.

Who should undergo this test?
Individuals with unexplained congenital hearing loss, family history of hearing disorders, or suspected inner ear malformations may be recommended this test.

Do I need any preparation before the test?
No fasting or special preparation is needed.

How long will the report take?
Results are usually available within a few working days depending on laboratory workflow.

How do the results help?
They assist clinicians in planning management strategies, evaluating cochlear implant suitability, and offering genetic counseling to families

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