Ophthalmology Genetics tests in Dubai & UAE

Compare available Ophthalmology 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

Listed price range

2,800.00–3,200.00 AED

Clinical preparation

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Ophthalmology Genetics test prices

Showing 1–7 of 7 matching tests.

Ophthalmology Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3510 CYP4V2 Gene Analysis for Bietti Crystalline Corneoretinal Dystrophy (Genetic Test) This genetic test identifies pathogenic variants in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy.	Peripheral whole blood (EDTA) 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 CYP4V2 gene", "Copy number variants (CNVs) within the CYP4V2 gene"] Parameters [] Preparation ["No specific fasting required.", "No specific medication or diet restrictions."] Indications ["Suspected Bietti crystalline corneoretinal dystrophy", "Family screening for Bietti crystalline corneoretinal dystrophy", "Reproductive planning for families affected by Bietti crystalline corneoretinal dystrophy"] Measurement technique Confirm with laboratory Codes LOINC: 21663-8 ICD-10: H35.53 Clinical summary This genetic test identifies pathogenic variants in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy.
TEST-3491 FOXL2 Gene Blepharophimosis, Epicanthus Inversus, and Ptosis (BPES) Genetic Test This genetic test identifies pathogenic variants in the FOXL2 gene associated with Blepharophimosis, Epicanthus Inversus, and Ptosis Syndrome (BPES).	Peripheral whole blood (3–5 mL in EDTA tube), extracted genomic DNA (≥1 µg), or dried blood spot on FTA card	21–28 calendar days from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FOXL2 gene pathogenic variants", "Detection of mutations in coding exons, splice junctions, and deep intronic regions"] Parameters [] Preparation ["No fasting required", "No medication adjustments needed", "Provide complete medical history"] Indications ["Suspected diagnosis of BPES", "Differentiation between BPES type I and type II", "Reproductive risk counselling", "Predictive testing in at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 102037-7 ICD-10: Q10.7 Clinical summary This genetic test identifies pathogenic variants in the FOXL2 gene associated with Blepharophimosis, Epicanthus Inversus, and Ptosis Syndrome (BPES).
TEST-3520 FYCO1 Gene Genetic Test (Autosomal Recessive Congenital Cataract Type 2) This test evaluates the FYCO1 gene for pathogenic variants associated with autosomal recessive congenital cataract type 2.	Peripheral Whole Blood (EDTA) or Dried Blood Spot (FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FYCO1 gene sequence", "Pathogenic variants in FYCO1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected autosomal recessive congenital cataract type 2", "Family history of congenital cataracts"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q12.0 Clinical summary This test evaluates the FYCO1 gene for pathogenic variants associated with autosomal recessive congenital cataract type 2.
TEST-2740 Microphthalmia / Anophthalmia / Coloboma Spectrum (MAC) Genetic Sequencing Test This test evaluates for genetic variants associated with microphthalmia, anophthalmia, and coloboma spectrum disorders.	Peripheral Whole Blood	45 Working Days	3,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants in genes associated with MAC", "Copy number variations (CNVs) in relevant genes"] Parameters [] Preparation [] Indications ["Patients presenting with microphthalmia, anophthalmia, or coloboma", "Family history of MAC spectrum disorders", "Need for genetic counselling regarding congenital eye anomalies"] Measurement technique Confirm with laboratory Codes LOINC: 93841-4 ICD-10: Q11.1, Q11.0, Q14.8 Clinical summary This test evaluates for genetic variants associated with microphthalmia, anophthalmia, and coloboma spectrum disorders.
TEST-3499 PAX6 Gene Aniridia Next-Generation Sequencing (NGS) Genetic Test This test identifies genetic mutations in the PAX6 gene associated with congenital aniridia.	Peripheral whole blood (EDTA), extracted genomic 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 ["PAX6 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Individuals with clinical features of aniridia", "Individuals with a documented family history of aniridia", "Couples planning a pregnancy who wish to understand recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q13.1, H54.0, H54.1 Clinical summary This test identifies genetic mutations in the PAX6 gene associated with congenital aniridia.
TEST-3481 PDE6H Gene Achromatopsia Type 6 Genetic Test This test identifies pathogenic variants in the PDE6H gene associated with autosomal recessive achromatopsia type 6.	Peripheral Whole Blood (EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDE6H gene mutations", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected achromatopsia type 6", "Family history of achromatopsia", "Congenital visual impairment"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H53.51, H35.5 Clinical summary This test identifies pathogenic variants in the PDE6H gene associated with autosomal recessive achromatopsia type 6.
TEST-3573 POC1B Gene Cone-Rod Dystrophy Type 20 Genetic Test This genetic test identifies pathogenic variants in the POC1B gene associated with cone-rod dystrophy type 20.	Peripheral whole blood or FTA card specimen	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 POC1B gene", "Inherited retinal disorder risk"] Parameters [] Preparation ["No special fasting required"] Indications ["Clinical suspicion of cone-rod dystrophy type 20", "Family history of inherited retinal disorders", "Guiding ophthalmologic management", "Informing family planning decisions"] Measurement technique Confirm with laboratory Codes LOINC: 94754-3 ICD-10: H35.54 Clinical summary This genetic test identifies pathogenic variants in the POC1B gene associated with cone-rod dystrophy type 20.

Category overview

Ophthalmology Genetics: overview

Safeguarding your family’s ocular health starts with a deep understanding of your hereditary blueprint, giving you the power to make highly informed decisions. As an elite component of our advanced Genetics department, comprehensive Ophthalmology Genetics screening provides an in-depth evaluation of the diverse pathways governing eye structure and function. Utilizing state-of-the-art diagnostic technology, this expansive genomic testing uncovers inherited susceptibilities to degenerative eye conditions, safely guiding customized medical oversight and early therapeutic interventions. Consistently trusted by patients and specialists across premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic accuracy, and rapid turnaround times. Take control of your visual health journey—book your ophthalmology genetics testing in UAE, arrange a secure home sample collection, or consult our specialized genetics 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.