Test Price
2,800 AEDโ Home Collection Available
CEP63 Gene Microcephaly Genetic Test in Dubai | 2800 AED | DNA Labs UAE
Executive Summary & Core Metrics
The CEP63 Gene Microcephaly NGS Test offers 99.9% diagnostic sensitivity via ISO-accredited processing, identifying pathogenic variants linked to autosomal recessive primary microcephaly and Seckel syndrome.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy and Temperature-Controlled Cold-Chain Home Collection (Available daily 8 AM โ 11 PM).
- Clinical Guidance: Telephonic Post-Test Guidance in result interpretation from a Consultant Medical Geneticist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The CEP63 Gene Microcephaly NGS Test analyzes the entire coding region of the CEP63 gene using Next-Generation Sequencing to identify pathogenic variants linked to autosomal recessive primary microcephaly and Seckel syndrome. It sequences the full gene including splice sites to detect single nucleotide variants, small deletions, and copy number changes.
| Features | Our CEP63 NGS Test | Alternative: Single-Gene Sanger Sequencing |
|---|---|---|
| Methodology | Next-Generation Sequencing (NGS) | Sanger Sequencing |
| Turnaround Time | 3โ4 Weeks | 6โ8 Weeks |
| Variant Detection | Full gene (exons + splice sites) | Limited to selected exons |
| Price (AED) | 2,800 | ~3,500 (varies) |
Physician Insight & Safety Protocols
โAs a Consultant Medical Geneticist, I emphasize that a CEP63 variant report must be interpreted in the context of the patientโs full dysmorphology evaluation and family history. A positive result can confirm a diagnosis of CEP63-related microcephaly, guiding early intervention and family counseling, but a negative result does not exclude other genetic causes. Telephonic post-test guidance ensures you understand results and next steps.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory: Safety Protocols and Precautions
This genetic test is a non-invasive blood draw or buccal swab. No special preparation is required. All sample collections follow ISO 15189:2022 standards. In case of a blood draw, standard precautions for venipuncture are observed. If a patient has a known bleeding disorder, a buccal swab or FTA card sample is recommended. Do not discontinue any prescribed medication based on genetic test results without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Inability of legal guardian to provide informed consent for minors; absence of documented microcephaly (head circumference < -2 SD for age and sex) or relevant dysmorphic features; active coagulopathy unless sample is collected via buccal swab or FTA card.
- Turnaround Caution: Not suitable for emergency prenatal diagnosis; turnaround time is 3โ4 weeks.
- Emergency Red Flags: Seek immediate medical care if the patient develops seizures, loss of consciousness, or signs of anaphylaxis (rash, swelling, breathing difficulty) after sample collection. These are unrelated to the test but require urgent attention.
Patient FAQ & Clinical Guidance
1. What does the CEP63 genetic test diagnose?
Direct Answer: This test identifies mutations in the CEP63 gene causing autosomal recessive primary microcephaly and Seckel syndrome, aiding precise clinical management. It sequences the entire gene to detect single nucleotide variants, small deletions, and copy number changes.
2. How is the sample collected for the test in the UAE?
Direct Answer: A certified phlebotomist collects 2โ3 mL of whole blood or a painless finger-prick blood spot on an FTA card at your home. The sample is transported in a temperature-controlled cold chain to our ISO-certified lab. VIP Mobile Phlebotomy is available daily from 8 AM to 11 PM.
3. Is this test covered by insurance or mandated by DHA regulations?
Direct Answer: We verify direct billing eligibility with major UAE insurers via WhatsApp. Under DHA guidelines, genetic testing requires informed consent and a clinical indication. The test is not mandatory but is recommended for children with microcephaly under specialist care.
4. What should I do after receiving the test results?
Direct Answer: Our Consultant Medical Geneticist provides a telephonic post-test guidance session to interpret results, discuss implications for family planning, and recommend further evaluations if necessary. If the result is positive, genetic counseling is strongly advised.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance: This service adheres to 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. Clinical safety and patient consent comply with Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory is ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139). DHA Facility License: 1143. All genetic data is handled with strict confidentiality and security.
Clinical & Logistical Metadata
| Test Name | CEP63 Gene Microcephaly NGS Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Whole Blood (2-3 mL) or Buccal Swab / FTA Card |
| Methodology Used | Next-Generation Sequencing (NGS) โ Full Gene Sequencing |
| ICD-10-CM Code | Q02 (Microcephaly), Q87.1 (Seckel syndrome) |
| LOINC Code | 55232-0 (CEP63 gene mutation analysis) |
| DHA Facility License & Address | DHA Facility License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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All reports reviewed by DHA-Certified physicians