Genetic Deafness tests in Dubai & UAE

Compare available Genetic Deafness 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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Genetic Deafness test prices

Showing 1–4 of 4 matching tests.

Genetic Deafness diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5580 CABP2 Gene (Autosomal Recessive Deafness Type 93) Genetic Test This test identifies pathogenic variants in the CABP2 gene associated with autosomal recessive deafness type 93 (DFNB93).	Whole blood (EDTA), extracted DNA, or FTA card	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CABP2 gene", "Presence of mutations associated with DFNB93"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Individuals with congenital or early-onset sensorineural hearing loss", "Family history of hereditary hearing loss", "Consanguinity"] Measurement technique Confirm with laboratory Codes LOINC: 83325-1 ICD-10: H90.3 Clinical summary This test identifies pathogenic variants in the CABP2 gene associated with autosomal recessive deafness type 93 (DFNB93).
TEST-5658 MSRB3 Gene Autosomal Recessive Deafness Type 74 (DFNB74) Genetic Test This genetic test evaluates the MSRB3 gene for mutations associated with autosomal recessive non-syndromic hearing loss (DFNB74).	Peripheral Whole Blood (EDTA)	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MSRB3 gene mutations", "Point mutations", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation [] Indications ["Individuals with congenital bilateral sensorineural hearing loss", "Family history of autosomal recessive inheritance", "Consanguinity", "Carrier testing for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21756-8 ICD-10: H90.5 Clinical summary This genetic test evaluates the MSRB3 gene for mutations associated with autosomal recessive non-syndromic hearing loss (DFNB74).
TEST-5703 SLC17A8 Gene Deafness, Autosomal Dominant Type 25 Genetic Test This test evaluates the SLC17A8 gene for pathogenic variants associated with autosomal dominant nonsyndromic hearing loss (DFNA25). It uses Next-Generation Sequencing (NGS) to anal...	Whole Blood (Peripheral) or Buccal Swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC17A8 gene", "Coding sequence analysis"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of autosomal dominant nonsyndromic hearing loss (DFNA25)", "Familial cascade testing for DFNA25", "Genetic counseling for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 54339-1 ICD-10: H90.5 Clinical summary This test evaluates the SLC17A8 gene for pathogenic variants associated with autosomal dominant nonsyndromic hearing loss (DFNA25). It uses Next-Generation Sequencing (NGS) to analyze the full coding region.
TEST-5696 TMC1 Gene Deafness (Autosomal Dominant Type 36) Genetic Test This test identifies pathogenic variants in the TMC1 gene associated with autosomal dominant non-syndromic hearing loss (DFNA36).	Whole Blood, Extracted DNA, One-drop Blood on FTA Card	3–4 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", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform the lab of any current medications"] Indications ["Diagnosis of autosomal dominant non-syndromic hearing loss (DFNA36)", "Genetic counselling for families with hearing loss", "Assessment of inheritance risk for family members"] Measurement technique Confirm with laboratory Codes LOINC: 82467-3 ICD-10: H90.3, H91.9 Clinical summary This test identifies pathogenic variants in the TMC1 gene associated with autosomal dominant non-syndromic hearing loss (DFNA36).

Category overview

Genetic Deafness: overview

Discovering unexpected hearing loss in a newborn or experiencing progressive auditory decline requires finding the exact biological root to map out an effective intervention plan. Within our specialized Genetics department, Genetic Deafness testing evaluates your DNA for the most common inherited mutations—such as those in the GJB2 gene—that disrupt the delicate structures of the inner ear. Utilizing advanced diagnostic technology, this vital molecular screening helps differentiate hereditary hearing loss from environmental factors, safely guiding personalized audiology care, cochlear implant planning, and early educational support. Recognized for compassionate sensory diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, exceptional analytical precision, and prompt reporting. Support your family's auditory health—book your genetic deafness testing in UAE, arrange a secure home sample collection, or consult our dedicated specialists.

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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.