Test Price
2,800 AED✅ Home Collection Available
TCOF1 Gene (Treacher Collins Syndrome Type 1) Genetic Test in UAE – DHA Licensed
Executive Summary & Core Metrics
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy (available daily 8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The TCOF1 gene test utilizes Next Generation Sequencing (NGS) to detect pathogenic variants linked to Treacher Collins syndrome type 1, a rare craniofacial disorder. This analysis covers the entire coding region and splice sites, delivering comprehensive molecular insight.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | NGS (Next Generation Sequencing) | Sanger Sequencing |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks |
| Price | 2,800 AED | 2,100 AED (Typically) |
| Clinical Depth | Comprehensive (entire coding region + splice sites) | Limited to specific known point mutations |
Physician Insight & Safety Protocols
“As a Consultant Medical Geneticist, I emphasize that TCOF1 gene test results must be interpreted within the full clinical context including family history. A negative result does not exclude all genetic causes of craniofacial disorders. Comprehensive pre- and post-test genetic counseling is essential for affected families and their healthcare providers.” – Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Advisory: Medication Continuation
Do not discontinue any prescribed medication without first consulting your physician. The genetic test does not replace ongoing clinical management.
Safety Exclusions & Red Flags
- Exclusion: Individuals under 18 years without legal guardian consent (per Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Exclusion: Active infection or acute illness requiring immediate medical attention.
- Red Flag: Sudden respiratory distress, stridor, or cyanosis – seek emergency care immediately.
- Red Flag: Severe feeding difficulties or airway obstruction in infants – urgent pediatric consultation required.
Patient FAQ & Clinical Guidance
1. What is the TCOF1 gene test and why is it needed?
This advanced NGS test precisely detects TCOF1 gene mutations causing Treacher Collins syndrome type 1. It is essential for confirming craniofacial dysmorphology diagnoses, guiding early surgical planning, and providing accurate recurrence risk to families. Pediatricians and clinical geneticists recommend it when facial malformations are suspected.
2. How is the sample collected and what preparation is needed?
A peripheral blood sample (or FTA card) is collected at your home by a certified phlebotomist using ISO-certified cold-chain logistics. No fasting is required; however, a prior genetic counseling session to document family pedigree is mandatory. Pre-clinical history documentation ensures optimal analytical sensitivity.
3. When will I receive the results and how reliable are they?
Results are delivered within 3 to 4 weeks after thorough NGS analysis. Our ISO-accredited laboratory achieves greater than 99.9% analytical sensitivity and specificity. Reports include detailed variant interpretation aligned with DHA guidelines, and a teleconsultation is offered to discuss findings and next steps.
UAE Regulatory & Data Privacy Adherence
Your Privacy & Legal Safeguards
All personal data handling complies 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 information is processed under strict confidentiality and consent protocols as mandated by DHA regulatory frameworks.
Clinical & Logistical Metadata
| Test Name | TCOF1 Gene (Treacher Collins Syndrome Type 1) Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral blood or FTA card (VIP Mobile Phlebotomy and cold-chain home collection available 8 AM – 11 PM daily) |
| Methodology Used | Next Generation Sequencing (NGS) |
| ICD-10-CM Code | Q75.4 |
| LOINC Code | 21647-4 |
| DHA Facility License & Laboratory Address | DHA License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians