Hearing Loss Genetics tests in Dubai & UAE

Compare available Hearing Loss Genetics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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Listed price range

2,800.00 AED

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Hearing Loss Genetics test prices

Showing 16–20 of 20 matching tests.

Hearing Loss Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5593 SLC26A4 Gene Pendred Syndrome Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC26A4 gene", "Single-nucleotide variants", "Small insertions or deletions", "Copy number variations (CNV)"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session", "Written informed consent required (guardian for minors)"] Indications ["Clinical suspicion of Pendred syndrome", "Hereditary sensorineural hearing loss", "Family history of Pendred syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81348-3 ICD-10: E07.1 Clinical summary This test evaluates the entire coding region and conserved splice sites of the SLC26A4 gene for pathogenic variants associated with Pendred syndrome.
TEST-5665 SUN1 Gene Genetic Test for Autosomal Recessive Deafness 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SUN1 gene sequence", "Pathogenic variants (point mutations, small insertions/deletions, copy number variations)"] Parameters [] Preparation ["No fasting required", "Provide detailed hearing-loss history", "Attend a genetic counseling session beforehand", "Inform of any recent blood transfusions"] Indications ["Diagnosis of autosomal recessive non-syndromic sensorineural hearing loss", "Family planning for individuals with a family history of hearing loss", "Genetic counseling for hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H90.3, H90.41, H90.42 Clinical summary This test identifies pathogenic variants in the SUN1 gene associated with autosomal recessive non-syndromic sensorineural hearing loss.
TEST-5599 SYNE4 Gene Deafness (Autosomal Recessive Type 76) Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SYNE4 gene variants", "Pathogenic mutations", "Likely pathogenic mutations"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Individuals with congenital or early-onset sensorineural hearing loss of unknown etiology", "Families with a history of autosomal recessive deafness", "Couples planning a family who are known carriers of a SYNE4 variant", "Individuals seeking clarification of a previous inconclusive genetic result", "Prenatal or preimplantation genetic testing in at-risk couples"] Measurement technique Confirm with laboratory Codes LOINC: 101430-9 ICD-10: H90.3 Clinical summary This genetic test identifies pathogenic variants in the SYNE4 gene associated with autosomal recessive hearing loss (DFNB76).
TEST-5659 TMC1 Gene Deafness Autosomal Recessive Type 7 Genetic Test This genetic test identifies pathogenic variants in the TMC1 gene associated with autosomal recessive non-syndromic hearing loss type 7 (DFNB7). It detects mutations causing severe...	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TMC1 gene", "Copy number variations (CNVs) in the TMC1 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Individuals with congenital or early-onset bilateral hearing loss", "Family history suggesting recessive inheritance of hearing loss", "Preconception carrier screening for couples"] Measurement technique Confirm with laboratory Codes LOINC: 101371-1 ICD-10: H90.3 Clinical summary This genetic test identifies pathogenic variants in the TMC1 gene associated with autosomal recessive non-syndromic hearing loss type 7 (DFNB7). It detects mutations causing severe-to-profound bilateral sensorineural deafness.
TEST-5648 TMPRSS3 Gene Deafness, Autosomal Recessive Type 8/10 Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMPRSS3 gene sequence", "Pathogenic variants in TMPRSS3"] Parameters [] Preparation [] Indications ["Diagnosis of autosomal recessive nonsyndromic hearing loss (DFNB8/DFNB10)", "Genetic counseling for families with hereditary deafness", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: H90.3 Clinical summary This test evaluates the TMPRSS3 gene for mutations associated with autosomal recessive nonsyndromic hearing loss types DFNB8 and DFNB10.

Category overview

Hearing Loss Genetics: overview

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.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.