Test Price
2,800 AED✅ Home Collection Available
SLC26A2 Gene Achondrogenesis Type 1B Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited NGS processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily 8 AM–11 PM).
- Clinical Guidance: Complimentary telephonic post-test clinical guidance with result interpretation by DHA-licensed genetic specialists.
- Insurance Support: Direct Billing Verification available via WhatsApp at +971 54 548 8731.
- DHA Facility License: 1143 | Corporate Lab: DNA Labs UAE
Test Overview & Methodology
This genetic test provides comprehensive molecular analysis of the SLC26A2 gene to confirm or rule out Achondrogenesis Type 1B, a lethal autosomal recessive skeletal dysplasia. The test is indicated for prenatal and postnatal diagnosis, carrier screening, and family risk assessment. Our platform employs Next Generation Sequencing (NGS) with Sanger confirmation, offering full gene coverage and copy number variant detection.
| Feature | Our NGS Test (ISO 9001:2015) | Standard Genetic Test (Alternative) |
|---|---|---|
| Precision | Full gene sequencing with copy number variant detection (99.9% sensitivity) | Targeted mutation analysis only (lower sensitivity, misses novel variants) |
| Methodology | Next Generation Sequencing (NGS) with Sanger confirmation | Sanger sequencing of select exons or PCR‑based panels |
| Turnaround Time | 3–4 Weeks (expedited reporting upon request) | 6–8 Weeks |
Physician Insight & Safety Protocols
“As a clinical geneticist, I emphasize that this test delivers definitive molecular confirmation for Achondrogenesis Type 1B. However, results must be correlated with imaging and family history. I strongly advise all patients to undergo pre-test genetic counseling and to review results with a qualified genetic counselor or physician for informed reproductive decisions.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Pre-Test Genetic Counseling Requirement
Advisory: Federal Decree-Law No. 4 of 2016 on Medical Liability mandates that all genetic tests with significant health implications be preceded by informed consent and genetic counseling. This test is offered only after a documented counseling session with a DHA-licensed genetic professional.
Safety & Exclusion Criteria
Contraindications and Precautions
- Minors (under 18): Testing permitted only with legal guardian consent and mandatory pre‑test genetic counseling, in compliance with UAE regulations.
- Patients with bleeding disorders or those on anticoagulant therapy must inform the phlebotomist to adapt the collection procedure.
- Pregnant individuals requiring prenatal testing must have a referral from a fetal medicine specialist.
- Emergency Red Flags: If you experience severe dizziness, uncontrolled bleeding, or signs of infection at the sample site, seek immediate medical attention.
Patient FAQ & Clinical Guidance
1. What is the SLC26A2 gene and Achondrogenesis Type 1B?
The SLC26A2 gene encodes a sulfate transporter essential for normal cartilage development. Pathogenic variants cause Achondrogenesis Type 1B, a severe autosomal recessive skeletal dysplasia characterized by extreme shortening of limbs, narrow thorax, and lethal respiratory insufficiency. This NGS test detects all known and novel variants with 99.9% sensitivity, confirming the diagnosis and enabling precise recurrence risk counseling for families.
2. Who should consider this genetic test?
This test is recommended for individuals with a family history of skeletal dysplasia, prenatal ultrasound findings suggestive of achondrogenesis, couples planning a pregnancy who are known carriers of SLC26A2 mutations, and individuals seeking definitive molecular diagnosis to guide reproductive decisions. Clinical supervision and genetic counseling are mandatory before and after testing.
3. How is the sample collected and what is the turnaround time?
A small peripheral whole blood sample is collected by a DHA‑licensed phlebotomist. For home collection, our VIP Mobile Phlebotomy service is available daily from 8 AM to 11 PM, with temperature‑controlled cold‑chain transport. The laboratory analysis takes 3–4 weeks, with expedited reporting available upon request.
UAE Regulatory & Data Privacy Adherence
This test and its associated data handling comply fully with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – ensuring secure processing and storage of your genetic information.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – governing electronic health records and telehealth interactions.
- Federal Decree-Law No. 4 of 2016 on Medical Liability – regulating clinician accountability and informed consent for genetic testing.
Your results are encrypted, accessible only to authorized medical staff, and never shared without your explicit consent.
Clinical & Logistical Metadata
| Test Name | SLC26A2 Gene Sequencing (Achondrogenesis Type 1B) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks (expedited available) |
| Sample Type / Matrix | Peripheral whole blood (or extracted DNA) |
| Methodology Used | Next Generation Sequencing (NGS) with Sanger confirmation |
| ICD-10-CM Code | Q77.0 (Achondrogenesis) |
| LOINC Code | 76076-3 (SLC26A2 gene mutation analysis) |
| DHA Facility License & Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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