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Diagnostic options ยท UAE

Ophthalmic Genetics tests in Dubai & UAE

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

Tests in this category

5

Listed price range

2,800.00โ€“3,200.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Ophthalmic Genetics test prices

Showing 1โ€“5 of 5 matching tests.

Ophthalmic Genetics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-3611
CACNA1F Gene Cone-Rod Dystrophy, X-Linked Type 3 Genetic Test

This genetic test analyzes the CACNA1F gene for mutations associated with X-linked cone-rod dystrophy.

Peripheral Whole Blood (EDTA Tube) 3 to 4 Weeks (21 โ€“ 28 Business Days) 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic mutations in the CACNA1F gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy Number Variations (CNV)"]
Parameters
[]
Preparation
["No specific fasting required.", "Inform the lab of any medications being taken."]
Indications
["Suspected diagnosis of X-linked cone-rod dystrophy", "Family history of cone-rod dystrophy", "Need for genetic counseling and recurrence risk assessment", "Eligibility assessment for gene therapy clinical trials"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94233-3 ICD-10: H35.54
Clinical summary
This genetic test analyzes the CACNA1F gene for mutations associated with X-linked cone-rod dystrophy.
TEST-3531
HSF4 Gene Cataract (Lamellar) Genetic Test

This test evaluates the HSF4 gene for pathogenic variants associated with congenital lamellar cataract.

Peripheral Blood or Buccal Swab 3โ€“4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["HSF4 gene coding region", "HSF4 gene splice-site boundaries"]
Parameters
[]
Preparation
[]
Indications
["Diagnosis of congenital lamellar cataract", "Cascade screening of at-risk family members", "Guiding surgical timing", "Prognostic counselling"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94306-4 ICD-10: Q12.0
Clinical summary
This test evaluates the HSF4 gene for pathogenic variants associated with congenital lamellar cataract.
TEST-3644
NDP Gene Exudative Vitreoretinopathy Type 2 (EVR2) Genetic Test

This genetic test identifies pathogenic variants in the NDP gene associated with Exudative Vitreoretinopathy Type 2 (EVR2).

Peripheral Whole Blood or Dried Blood Spot (FTA Card) 3 to 4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the NDP gene"]
Parameters
[]
Preparation
["Do not discontinue any prescribed medication without consulting your doctor.", "Inform our phlebotomist if you are taking anticoagulants or have a bleeding disorder.", "Fasting is not required."]
Indications
["Suspected Exudative Vitreoretinopathy Type 2 (EVR2)", "Family history of EVR2", "Need for genetic counseling and family planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: H35.029
Clinical summary
This genetic test identifies pathogenic variants in the NDP gene associated with Exudative Vitreoretinopathy Type 2 (EVR2).
TEST-2767
Ophthalmoplegia Genetic Panel (NGS) Test

This test detects pathogenic variants in genes linked to ophthalmoplegia and related mitochondrial disorders using NGS and Sanger sequencing.

Whole Blood (EDTA) 45 working days 3,200.00 AED
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What it measures
["Pathogenic variants in genes associated with ophthalmoplegia", "Mitochondrial DNA variants", "Indels", "CNVs"]
Parameters
[]
Preparation
["Fasting is not required", "Inform phlebotomist of anticoagulant therapy", "Do not discontinue prescribed medications without consulting physician"]
Indications
["Diagnosis of progressive external ophthalmoplegia", "Diagnosis of mitochondrial myopathies", "Diagnosis of congenital eye-muscle paralysis", "Familial risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94473-3 ICD-10: H49.81
Clinical summary
This test detects pathogenic variants in genes linked to ophthalmoplegia and related mitochondrial disorders using NGS and Sanger sequencing.
TEST-3674
WDR36 Gene Glaucoma (Open Angle Type 1G) Genetic Test

This test identifies mutations in the WDR36 gene associated with an increased risk of developing primary open-angle glaucoma type 1G.

Peripheral Whole Blood or Saliva 3โ€“4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["WDR36 gene mutations", "Genetic predisposition to primary open-angle glaucoma type 1G"]
Parameters
[]
Preparation
[]
Indications
["Family history of early-onset open-angle glaucoma", "Diagnosis of open-angle glaucoma under 50 years of age"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: H40.10, Z13.5, Z15.89
Clinical summary
This test identifies mutations in the WDR36 gene associated with an increased risk of developing primary open-angle glaucoma type 1G.

Category overview

Ophthalmic Genetics: overview

Understanding the hereditary risks affecting your familyโ€™s eye health empowers you to make proactive, highly informed decisions for long-term ocular wellness. As an elite component of our advanced Molecular Genetics services, comprehensive Ophthalmic Genetics screening provides an in-depth evaluation of the diverse genetic pathways that govern eye structure and function. Utilizing cutting-edge diagnostic technology, this expansive genomic testing delivers the critical clarity needed to uncover inherited susceptibilities, safely guiding customized medical monitoring and specialized therapeutic interventions. Consistently trusted by patients and specialists among premier diagnostic labs in the UAE, DNA Labs guarantees strict patient confidentiality, uncompromising diagnostic accuracy, and prompt reporting. Take control of your visual health journeyโ€”schedule your ophthalmic genetics testing in UAE, arrange a comfortable home sample collection, or consult our dedicated genetics specialists today.

Before booking

Use the test details as a conversation starter

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.