Test Price
2,800 AED✅ Home Collection Available
AIPL1 Gene Cone-Rod Dystrophy Genetic Testing (NGS) in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Why UAE Families Choose Our AIPL1 Gene Test
Achieve 99.9% diagnostic sensitivity with our ISO‑accredited NGS test. Benefit from premium mobile phlebotomy with temperature‑controlled cold‑chain home collection (daily 8 AM – 11 PM) and expert post‑test genetic counselling. Insurance verification via WhatsApp: +971 54 548 8731. Test price: 2,800 AED (includes mandatory pre‑test counselling). Turnaround time: 3–4 weeks with clinical urgency option. Full compliance with UAE Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
Test Overview & Methodology
The AIPL1 gene test analyzes inherited cone‑rod dystrophy using next‑generation sequencing (NGS), providing definitive diagnosis and carrier status. This test identifies pathogenic variants in the AIPL1 gene linked to progressive vision loss, enabling targeted clinical management and genetic counselling. The NGS panel covers the entire coding region plus flanking intronic sequences, detecting single nucleotide variants, small insertions/deletions, and copy number variants (with MLPA backup).
| Feature | Our NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Molecular Method | High‑coverage NGS (full gene & flanking regions) | Single‑amplicon Sanger |
| Variants Detected | SNVs, indels, copy number variants (MLPA backup) | Only known point mutations |
| Turnaround Time | 3–4 weeks (with clinical urgency option) | Up to 8 weeks |
| Pre‑Test Counselling | Mandatory, included in cost | Often separate |
Physician Insight & Safety Protocols
“Genetic testing for AIPL1 provides crucial clarity for families affected by cone‑rod dystrophy, but it must be interpreted within the full clinical and family context. A positive result confirms the diagnosis; a negative result does not exclude all inherited retinal conditions. Always collaborate with a clinical geneticist and ophthalmologist to integrate these findings into a personalised care plan.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics – DHA Registration ID: 9294403
Medication & Clinical Decision Advisory
Do not alter any prescribed treatment solely based on genetic results. Changes to medication, supplements, or lifestyle should always be discussed with your consulting physician. Genetic findings are one piece of the diagnostic puzzle; they do not replace regular clinical examinations or specialist advice.
Patient Safety: Exclusion Criteria & Red Flags
- Exclusion Criteria: Minors require explicit consent from a legal guardian. Patients currently unable to provide informed consent due to acute medical or psychiatric condition are ineligible until cleared by a physician.
- Red Flags – Seek Immediate Emergency Care: Sudden severe vision loss, acute ocular pain, or eye redness with light sensitivity. Do not wait for genetic testing; proceed directly to the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What does the AIPL1 gene test actually detect?
The AIPL1 gene test detects pathogenic mutations in the AIPL1 gene, confirming a diagnosis of cone‑rod dystrophy and clarifying carrier status. Using NGS, it screens the entire coding region and flanking introns for single nucleotide variants, small insertions/deletions, and larger copy number variations. This information is essential for predicting disease progression, assessing recurrence risk, and guiding family planning decisions.
2. Is genetic counselling mandatory before this test?
Yes, a pre‑test genetic counselling session is mandatory to construct a detailed family pedigree and ensure informed consent in accordance with UAE regulations. Our certified genetic counsellors explain the inheritance pattern, possible outcomes, and psychosocial implications before any sample is collected. This session is included in the test price and can be conducted via secure video consultation.
3. How long do results take and what support do I get after?
Results are available within 3 to 4 weeks through ISO‑certified NGS processing. A telephonic post‑test guidance session with the referring specialist is included at no extra cost. Your report will be explained in plain language, outlining next steps such as additional ophthalmic examinations, family cascade testing, and referral to support services. A written report in English is provided; Arabic translation is available on request.
UAE Regulatory & Data Privacy Adherence
This test and all patient data handling comply with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Genetic results are securely stored and shared only with the patient and their authorised healthcare provider. Clinical procedures adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability to ensure patient safety and informed consent. DNA Labs UAE is fully licensed by the Dubai Health Authority (DHA) under facility license number 1143.
Clinical & Logistical Metadata
| Test Name | AIPL1 Gene Cone‑Rod Dystrophy Genetic Testing (NGS) |
| Price (AED) | 2,800 AED (includes mandatory pre‑test counselling) |
| Turnaround Time | 3–4 weeks (clinical urgency option available) |
| Sample Type / Matrix | Peripheral whole blood (3–5 mL in EDTA tube). VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily from 8 AM to 11 PM. |
| Methodology Used | Next‑Generation Sequencing (NGS) – high‑coverage whole gene sequencing with MLPA for CNV confirmation |
| ICD-10-CM Code | H35.54 |
| LOINC Code | 91831-1 |
| DHA Facility License & Laboratory Address | DNA Labs UAE – DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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