Test Price
2,800 AED✅ Home Collection Available
ABCA4 Gene Cone-Rod Dystrophy Type 3 Genetic Test | 2800 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Complimentary Telephonic Post-Test Genetic Counselling session with a DHA-licensed specialist.
- Insurance Billing: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This targeted Genetic Test deciphers pathogenic variants in the ABCA4 gene, enabling definitive molecular diagnosis of Cone-Rod Dystrophy Type 3. It empowers ophthalmologists, genetic counsellors, and researchers with carrier screening and precise prognostic data, aligned with ACMG/AMP variant interpretation guidelines.
| Feature | Our ABCA4 NGS Test | Closest Alternative (WES) |
|---|---|---|
| Precision | 99.9% analytical sensitivity for ABCA4 coding exons ±20bp splice regions | Variable coverage; often requires orthogonal validation |
| Methodology | NGS with CNV calling & deep intronic analysis | Whole Exome Sequencing (may miss deep intronic variants) |
| Turnaround | 3 to 4 Weeks | 8–12 Weeks (with interpretation delays) |
| Clinical Report | DHA-compliant, includes pedigree integration & therapeutic eligibility | Generic VCF; often lacks ophthalmology-specific annotation |
Physician Insight & Safety Protocols
“As a Consultant Medical Genetics, I emphasize that ABCA4 results must be integrated with full clinical phenotyping, including electroretinography and family pedigree analysis. A comprehensive genetic report not only diagnoses Cone-Rod Dystrophy Type 3 but also guides family planning and potential eligibility for emerging gene therapies. My team ensures you receive clear, actionable insights.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue any prescribed eye medication, vitamin supplements, or systemic therapy without consulting your supervising ophthalmologist or genetic specialist. Abrupt cessation can trigger irreversible vision loss. This test is an elective diagnostic procedure and should not replace emergency medical care.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusions: Active ocular infection, recent intraocular surgery (<4 weeks), inability to provide informed genetic consent (minors require legal guardian approval per Federal Law No. 2 of 2019).
- Emergency Flags: Sudden loss of vision, acute eye pain, photopsia for >5 minutes, or floaters with flashes—proceed directly to your emergency ophthalmologist, not this elective test.
- Data Safety: All genetic data is encrypted per Federal Decree-Law No. 45 of 2021 (PDPL), stored on local servers; re-identification risk is legally minimized.
- Medical Liability: This procedure adheres strictly to the standards set forth in Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient safety and clinical accountability.
Patient FAQ & Clinical Guidance
1. Why does this test require genetic counselling before and after the blood draw?
Pre-test counselling captures a detailed pedigree, assesses autosomal recessive inheritance patterns, and prepares you psychologically for the results. Post-test counselling translates the complex NGS report into actionable medical steps and family planning options, fully aligned with DHA’s genomics consent standards.
2. Can this test be used for asymptomatic relatives or minors?
Predictive testing for at-risk family members is permitted only with comprehensive genetic counselling and, for minors, a court order or explicit medical necessity as defined by UAE regulations. Carrier screening for reproductive partners follows a separate DHA protocol.
3. How does the 2800 AED price compare to international costs, and is insurance accepted?
This fee covers NGS library preparation, sequencing, bioinformatics, clinical report, and one post-test teleconsult. International labs often charge 1500–3000 USD. We offer direct insurance billing with most UAE networks; please verify via WhatsApp at +971 54 548 8731 prior to collection.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates in full compliance with the United Arab Emirates’ stringent data protection and healthcare regulations. Your genetic data is handled securely under the following frameworks:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL): Ensuring your consent, data minimization, and rights to access or delete your genomic information.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields: Guaranteeing the confidentiality and cybersecurity of your electronic health records and genetic test results.
- ISO 9001:2015 Certification: Cert: INT/EGQ/2509DA/3139, confirming our quality management system meets international standards for laboratory operations and customer service.
Clinical & Logistical Metadata
| Test Name | ABCA4 Gene Cone-Rod Dystrophy Type 3 Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (3-5 ml EDTA) or Saliva (Oragene DNA Kit). Equivocal results may prompt a second blood draw for orthogonal confirmation. |
| Methodology Used | Next-Generation Sequencing (NGS) with CNV calling and deep intronic variant analysis on the Illumina platform. |
| ICD-10-CM Code | H35.54, Z13.5, Z14.8 |
| LOINC Code | 48006-5 |
| DHA Facility License & Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians