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Genetics

Hearing Loss Genetics Tests in Dubai & UAE

Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.

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Hearing Loss Genetics investigations

All 20 investigations in this category are listed below.

Hearing Loss Genetics tests offered by DNA Labs UAE — compare specimen type, turnaround time and listed price. Preparation and clinical interpretation are confirmed with your clinician before collection.
Test What it measures Specimen Turnaround Price Book
CDH23 Gene Deafness, Autosomal Recessive Type 12 (DFNB12) Genetic Test TEST-5721 LOINC 81247-9 This genetic test analyzes the CDH23 gene to identify pathogenic variants associated with autosomal recessive non-syndromic hearing loss type 12 (DFNB... Peripheral Whole Blood (EDTA Tube) or FTA Card Spot 3–4 weeks 2,800.00 AED Details
DCDC2 Gene (Autosomal Recessive Deafness Type 66) Genetic Test TEST-5663 LOINC 55233-1 This test identifies pathogenic variants in the DCDC2 gene associated with autosomal recessive non-syndromic hearing loss (DFNB66). Whole blood (EDTA), extracted DNA, or FTA card 3–4 weeks 2,800.00 AED Details
DIAPH1 Gene (Deafness, Autosomal Dominant 1) Genetic Test TEST-5722 LOINC 94121-2 This genetic test identifies pathogenic variants in the DIAPH1 gene associated with autosomal dominant non-syndromic hearing loss (DFNA1). It analyzes... Whole Blood (EDTA), Extracted DNA, or Dry Blood Spot on FTA Card 3 to 4 Weeks from sample receipt 2,800.00 AED Details
ESRRB Gene Deafness (Autosomal Recessive Type 35) Genetic Test TEST-5687 LOINC 97163-3 This genetic test identifies pathogenic variants in the ESRRB gene associated with autosomal recessive deafness type 35. Whole blood (EDTA), extracted DNA, or FTA card (dried blood spot) 3–4 weeks 2,800.00 AED Details
EYA4 Gene (DFNA10) Autosomal Dominant Hearing Loss Genetic Test (NGS) TEST-5780 LOINC 94513-5 This test detects pathogenic variants in the EYA4 gene associated with autosomal dominant nonsyndromic sensorineural hearing loss. Whole blood (EDTA), dried blood spot (FTA card), or extracted DNA 3–4 weeks 2,800.00 AED Details
GJB2 Gene Deafness, Autosomal Recessive Type 1A Genetic Test TEST-5714 LOINC 60674-4 This diagnostic test evaluates the GJB2 gene for mutations associated with autosomal recessive deafness type 1A. Peripheral Whole Blood 3–4 Weeks 2,800.00 AED Details
GJB6 Gene Deafness, Autosomal Recessive Type 1B Genetic Test TEST-5651 LOINC 21651-9 This test analyzes the GJB6 gene for mutations associated with autosomal recessive sensorineural hearing loss. Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card) 3–4 Weeks 2,800.00 AED Details
GRXCR1 Gene NGS Test for Autosomal Recessive Deafness Type 25 (DFNB25) TEST-5700 LOINC 55324-5 This test identifies pathogenic variants in the GRXCR1 gene associated with autosomal recessive nonsyndromic hearing loss DFNB25. Peripheral whole blood (EDTA tube) 3–4 weeks 2,800.00 AED Details
GSDME (DFNA5) Gene NGS Sequencing for Autosomal Dominant Deafness Type 5 Test TEST-5738 LOINC 21636-6 This test identifies pathogenic variants in the GSDME gene associated with autosomal dominant non-syndromic hearing loss. Peripheral Whole Blood (EDTA) or Buccal Swab / Saliva 3 to 4 Weeks 2,800.00 AED Details
KCNQ4 Gene Sequencing (Autosomal Dominant Deafness Type 2A, DFNA2A) Test TEST-5699 LOINC 81327-2 This diagnostic test evaluates the KCNQ4 gene for pathogenic variants associated with autosomal dominant nonsyndromic sensorineural hearing loss type... Peripheral Whole Blood (EDTA) 3–4 Weeks 2,800.00 AED Details
MITF Gene Tietz Albinism‑Deafness Syndrome Genetic Test TEST-5472 LOINC 81438-1 This genetic test evaluates the MITF gene for pathogenic variants associated with Tietz syndrome. Whole blood, extracted DNA, or dried blood spot 3–4 Weeks 2,800.00 AED Details
MYH9 Gene (DFNA17) Autosomal Dominant Nonsyndromic Hearing Loss — Genetic Test TEST-5710 LOINC 60591-5 This test identifies pathogenic variants within the MYH9 gene associated with autosomal dominant nonsyndromic hearing loss (DFNA17). It uses Next-Gene... Peripheral blood, DNA, FTA card 3–4 weeks 2,800.00 AED Details
MYO7A Gene (Deafness, Autosomal Recessive Type 2) Genetic Test TEST-5709 LOINC 21656-9 This genetic test evaluates the MYO7A gene for pathogenic variants associated with autosomal recessive deafness type 2 (DFNB2) and Usher syndrome type... Whole Blood (EDTA Tube), Extracted DNA, or FTA Card Blood Spot 3 to 4 Weeks 2,800.00 AED Details
OTOA Gene Deafness, Autosomal Recessive Type 22 Genetic Test TEST-5649 LOINC 21636-6 This test detects pathogenic variants in the OTOA gene associated with autosomal recessive nonsyndromic sensorineural hearing loss type 22. Peripheral Whole Blood (EDTA) or Buccal Swab 3–4 Weeks 2,800.00 AED Details
POU4F3 Gene (Autosomal Dominant Deafness Type 52) Genetic Test TEST-5676 LOINC 94121-4 This test detects pathogenic variants in the POU4F3 gene associated with autosomal dominant non-syndromic hearing loss (DFNA52). It uses next-generati... Whole Blood, Extracted DNA, or FTA Card 3–4 Weeks 2,800.00 AED Details
SLC26A4 Gene Pendred Syndrome Genetic Test TEST-5593 LOINC 81348-3 This test evaluates the entire coding region and conserved splice sites of the SLC26A4 gene for pathogenic variants associated with Pendred syndrome. Peripheral Whole Blood (DNA extraction) 3 to 4 Weeks 2,800.00 AED Details
SUN1 Gene Genetic Test for Autosomal Recessive Deafness TEST-5665 LOINC 81247-9 This test identifies pathogenic variants in the SUN1 gene associated with autosomal recessive non-syndromic sensorineural hearing loss. Peripheral Whole Blood (3-5 mL in EDTA tube) or DNA FTA Card 3 to 4 Weeks 2,800.00 AED Details
SYNE4 Gene Deafness (Autosomal Recessive Type 76) Genetic Test TEST-5599 LOINC 101430-9 This genetic test identifies pathogenic variants in the SYNE4 gene associated with autosomal recessive hearing loss (DFNB76). Peripheral whole blood, buccal swab, or FTA card 3 to 4 weeks 2,800.00 AED Details
TMC1 Gene Deafness Autosomal Recessive Type 7 Genetic Test TEST-5659 LOINC 101371-1 This genetic test identifies pathogenic variants in the TMC1 gene associated with autosomal recessive non-syndromic hearing loss type 7 (DFNB7). It de... Peripheral Whole Blood 3 to 4 Weeks 2,800.00 AED Details
TMPRSS3 Gene Deafness, Autosomal Recessive Type 8/10 Genetic Test TEST-5648 LOINC 21636-6 This test evaluates the TMPRSS3 gene for mutations associated with autosomal recessive nonsyndromic hearing loss types DFNB8 and DFNB10. Peripheral whole blood (3-5 mL in EDTA tube) 3–4 Weeks (express available on request) 2,800.00 AED Details

Clinical overview

About Hearing Loss Genetics

Understanding the broader hereditary landscape of auditory health empowers you to make fully informed, proactive decisions for your child’s developmental future. Integrated into our advanced Genetics department, comprehensive Hearing Loss Genetics screening utilizes expansive panels to simultaneously evaluate dozens of genes linked to both syndromic and non-syndromic deafness. Utilizing state-of-the-art genomic profiling, this robust screening uncovers elusive genetic drivers, offering the exact clarity required to safely guide specialized multidisciplinary care, proactive vision or thyroid monitoring (for syndromic cases like Usher or Pendred syndromes), and customized early intervention therapies. Highly regarded for clinical excellence among diagnostic labs in Dubai and the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and remarkably fast turnaround times. Take an empowered step toward targeted support—schedule your hearing loss genetics testing in UAE, coordinate a secure clinical sample collection, or consult our expert medical team.

Before your appointment

Preparation & sample collection

Follow the instructions you are given

Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.

Bring your identification

A valid photo ID is required at collection so that your sample is matched correctly to your record.

Tell us about medicines

Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.

Ask before collection

If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.

Patient information

Frequently asked questions

Practical answers about Hearing Loss Genetics testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.

How do I choose the right Hearing Loss Genetics test?

The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.

What specimen is required?

Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.

Do you offer home sample collection in Dubai and the UAE?

Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.

How long do results take?

Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.

Is there anything I need to do before sample collection?

Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.

How will I receive my report?

Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.

About this clinical information

The information on this Hearing Loss Genetics page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.

  • Investigation names, specimen types and listed prices are reviewed against laboratory records.
  • Preparation guidance is indicative — confirm test-specific instructions before collection.
  • Content is updated when investigations, methods or reporting formats change.
  • Results are released to the patient and, on request, shared with the referring clinician.

Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.

We're here to help

Need help choosing a Hearing Loss Genetics test?

Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.

Call +971 54 548 8731
  • Home collection available across the UAE
  • Digital reports delivered securely
  • Confidential handling of every request

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