Hereditary Deafness tests in Dubai & UAE

Compare available Hereditary 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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Hereditary Deafness test prices

Showing 1–3 of 3 matching tests.

Hereditary Deafness diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5565 COL4A6 Gene Deafness, X-Linked Type 6 Genetic Test This genetic test analyzes the COL4A6 gene to identify pathogenic variants associated with X-linked deafness type 6.	Peripheral whole blood (EDTA), extracted DNA, or dried blood spot (FTA card)	3–4 weeks (from sample receipt)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the COL4A6 gene", "Copy Number Variations (CNVs) within the COL4A6 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Diagnosis of X-linked deafness type 6", "Carrier detection in females for reproductive planning", "Genetic counseling for families with hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 82812-2 ICD-10: Q80.9 Clinical summary This genetic test analyzes the COL4A6 gene to identify pathogenic variants associated with X-linked deafness type 6.
TEST-5746 CRYM Gene Deafness, Autosomal Dominant Type 40 Genetic Test This test evaluates the CRYM gene for pathogenic variants associated with autosomal dominant non-syndromic hearing loss (DFNA40). It identifies mutations that can cause progressive...	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 ["CRYM gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Suspected autosomal dominant non-syndromic hearing loss", "Family history of DFNA40", "Genetic counseling for hereditary hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 81408-0 ICD-10: H90.3 Clinical summary This test evaluates the CRYM gene for pathogenic variants associated with autosomal dominant non-syndromic hearing loss (DFNA40). It identifies mutations that can cause progressive sensorineural hearing loss.
TEST-5688 MYH14 Gene Deafness (Autosomal Dominant Type 4) Genetic Test This genetic test evaluates the MYH14 gene for pathogenic variants associated with autosomal dominant nonsyndromic hearing loss (DFNA4). It uses Next-Generation Sequencing (NGS) to...	Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	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 MYH14 gene", "Single nucleotide variants (SNVs)", "Small insertions or deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No fasting required", "No dietary restrictions", "No special preparation needed"] Indications ["Individuals with clinical suspicion of DFNA4", "Family members of known MYH14 variant carriers", "Cascade screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 81248-4 ICD-10: H90.3, Z13.71, Z15.89 Clinical summary This genetic test evaluates the MYH14 gene for pathogenic variants associated with autosomal dominant nonsyndromic hearing loss (DFNA4). It uses Next-Generation Sequencing (NGS) to detect various types of genetic alterations.

Category overview

Hereditary Deafness: overview

Addressing a family history of profound hearing loss or navigating unexpected auditory challenges in a newborn requires compassionate, highly precise diagnostic care to ensure they receive the best possible support. Within our elite Genetics department, Hereditary Deafness testing meticulously analyzes your DNA for the specific inherited mutations known to disrupt the development and function of the inner ear. By leveraging cutting-edge molecular technology, this critical diagnostic screening helps confirm the genetic basis of the condition, offering the exact clarity needed to safely guide personalized pediatric audiology interventions, proactive cochlear implant planning, and tailored educational support. Trusted for sensitive sensory diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, unparalleled diagnostic precision, and highly efficient reporting. Support your child’s auditory journey—schedule your hereditary deafness testing in UAE, coordinate a comfortable home sample collection, or consult our dedicated medical genetics professionals today.

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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.