Test Price
2,800 AED✅ Home Collection Available
CEP152 Gene Microcephaly (Autosomal Recessive Type 9) Genetic Test in UAE
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited processing.
- Premium Logistics: VIP Mobile Phlebotomy and temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic post-test genetic counselling included for result interpretation.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The CEP152 gene test identifies pathogenic variants causing autosomal recessive primary microcephaly type 9 (MCPH9), a rare neurodevelopmental disorder characterized by significantly reduced head circumference and intellectual disability. This advanced genetic test analyses the entire coding region of CEP152 using next-generation sequencing, enabling precise diagnosis, informed family planning, and targeted clinical management for affected children in the UAE.
| Feature | Our Test | Closest Alternative (UAE Competitor) |
|---|---|---|
| Precision | Full gene sequencing (NGS) with >99.9% analytical sensitivity | Targeted panel or microarray with lower resolution |
| Method | Next-generation sequencing (Illumina platform), Sanger confirmation | PCR-based targeted mutation analysis |
| Turnaround | 3 to 4 weeks with interim genetic counselling | 6–8 weeks, no telephonic updates |
Physician Insight & Safety Protocols
“As a DHA-licensed Consultant Medical Genetics, I emphasize that a positive CEP152 result must be correlated with clinical history and neuroradiological imaging. Primary microcephaly can arise from multifactorial causes including environmental exposures and other genetic loci; therefore this test is not a standalone verdict but a critical piece of the diagnostic puzzle. I encourage families to discuss all findings with their paediatrician and clinical geneticist for integrated care planning.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)
Advisory Guidance for Patients and Families
Do not discontinue prescribed medications or modify existing treatment plans based solely on the outcome of this genetic test. Any therapeutic adjustments must be reviewed and approved by your treating physician or clinical geneticist.
Safety and Exclusion Criteria
- Exclusion: Patients with known bone marrow failure or severe anaemia that contraindicates venipuncture.
- Exclusion: Refusal or inability to provide informed consent (including legal guardian consent for minors as required under UAE Federal Decree-Law No. 4 of 2016 on Medical Liability).
- ER Red Flags: Sudden onset of seizures, loss of developmental milestones, or acute respiratory distress after sample collection – seek immediate medical attention.
- Pre-Test Requirements: Clinical history documentation and a pre-test genetic counselling session to construct a three-generation pedigree chart are mandatory. Accepted samples: whole blood (3–5 mL in EDTA tube), DNA FTA card, or extracted DNA. Specimens must be transported at 2–8°C within 72 hours.
Patient FAQ & Clinical Guidance
1. What does a positive CEP152 test mean for my child’s development?
A positive result confirms a genetic cause of primary microcephaly, enabling early intervention therapies and tailored developmental support to optimise cognitive and physical outcomes. Your paediatrician and genetic specialist will use this information to create a personalised care plan that addresses your child’s specific needs.
2. How do I arrange home collection for this genetic test in Dubai or Abu Dhabi?
Our VIP mobile phlebotomy service covers all UAE emirates from 8 AM to 11 PM, with same-day cold-chain transport to the laboratory. Simply WhatsApp +971 54 548 8731 for booking and insurance verification.
3. Is this test covered by health insurance in the UAE for families with a history of microcephaly?
Most UAE insurers cover medically indicated genetic testing when pre-authorised. We provide direct billing verification within 24 hours via WhatsApp using your Emirates ID and doctor’s referral details.
4. What is the turnaround time for receiving my child’s results?
Results are delivered within 3 to 4 weeks from sample receipt. Interim genetic counselling updates are provided during this period to keep you informed of progress.
5. Can this test detect carriers in my family for future planning?
Yes, the test can identify heterozygous carriers of CEP152 pathogenic variants, which is valuable for recurrence risk assessment and reproductive planning. A pre-test genetic counselling session is mandatory to discuss implications for family members.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates in full compliance with the UAE’s legal framework for health data protection and genetic testing. All personal and clinical data are processed under 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. Patient consent, data confidentiality, and secure handling of genetic information are central to our laboratory practice.
Clinical & Logistical Metadata
| Test Name | CEP152 Gene Microcephaly (Autosomal Recessive Type 9) Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 weeks |
| Sample Type / Matrix | Whole blood (3–5 mL in EDTA tube), DNA FTA card, or extracted DNA |
| Methodology Used | Next-Generation Sequencing (Illumina platform) with Sanger confirmation |
| ICD-10-CM Code | Q02 |
| LOINC Code | 21636-6 |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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