EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test
Short Name: EYA4 DFNA10 NGS Test
Also known as: DFNA10, Autosomal Dominant Deafness Type 10, EYA4-Related Deafness
EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To detect mutations in the EYA4 gene associated with autosomal dominant deafness type 10 for diagnostic and counseling purposes.
- Test Code
- 2297
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation needed. Provide clinical history and family pedigree.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample collected via venipuncture or use of FTA card for one drop of blood.
Report Delivery
Sample sent to laboratory for NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the EYA4 gene associated with autosomal dominant deafness type 10 for diagnostic and counseling purposes.
How to Prepare
- Ensure proper sample labeling
- Use sterile collection equipment
- Store sample appropriately for transport
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for EYA4 mutations is crucial for accurate diagnosis and family counseling in cases of autosomal dominant deafness."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Improperly labeled sample
Understanding Your Results
If you experience progressive hearing loss, tinnitus, or balance problems, especially with a family history of deafness, consult an ENT specialist or geneticist.
Limitations
- ⚠May not detect all possible mutations
- ⚠Requires genetic counseling for interpretation
- ⚠Results may include variants of uncertain significance
Risks & Considerations
- ●Bruising at blood draw site
- ●Infection risk (minimal)
- ●Fainting during blood collection
Interfering Factors
- ●Poor sample quality
- ●Contamination
- ●Technical errors
Compare With Similar Tests
| Test | EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test | GJB2 Gene Test | SLC26A4 Gene Test | TMC1 Gene Test | Comprehensive Hearing Loss Panel |
|---|---|---|---|---|---|
| Comparison | EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test |
Frequently Asked Questions
What is EYA4 gene deafness?
What are the symptoms of DFNA10?
How is EYA4 gene deafness diagnosed?
What is NGS genetic testing?
What is the cost of the EYA4 gene deafness test?
Is home sample collection available?
How long does it take to get results?
Who should get this test?
Can insurance cover the test?
What are the treatment options for EYA4 gene deafness?
Is genetic counseling necessary?
How accurate is the test?
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₹20,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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