Test Price
2,800 AED✅ Home Collection Available
MSX2 Gene Parietal Foramina Type 1 Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Achieve 99.9% diagnostic sensitivity with ISO-certified NGS analysis for MSX2-related parietal foramina. Enjoy VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM – 11 PM, daily), with telephonic post-test clinical guidance. Insurance direct billing verification via WhatsApp at +971 54 548 8731.
Test price: 2,800 AED | Turnaround time: 3–4 weeks | Method: Next Generation Sequencing (NGS) covering full gene
Test Overview & Methodology
This targeted genetic test analyzes the MSX2 gene for pathogenic mutations causing parietal foramina type 1 (PFM1), a congenital skull ossification defect associated with craniofacial dysmorphology. Using Next Generation Sequencing (NGS), our technique provides single-nucleotide resolution across the entire coding region and splice sites, facilitating accurate variant detection for diagnosis, family cascade screening, and pediatric management. The analysis is performed at our ISO 9001:2015 accredited laboratory in Dubai Healthcare City.
| Feature | DNA Labs UAE – MSX2 NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | Single-nucleotide level detection, full gene coverage | Targeted exon analysis only |
| Method | Next Generation Sequencing (NGS) – high throughput | Sanger sequencing – low throughput |
| Speed | 3–4 weeks | 4–6 weeks |
| Clinical Utility | Comprehensive mutation identification including novel variants | Confirmation of known familial mutations only |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA ID: 9294403
“Genetic testing for MSX2-related parietal foramina requires careful clinical correlation with imaging and thorough pre- and post-test genetic counseling. The NGS platform offers excellent sensitivity for detection of causative mutations, yet carrier screening and family implications must be addressed through a structured dialogue. Our team ensures that every patient receives a personalized interpretation of results and a clear pathway for follow-up.”
Advisory – Medication & Sample Collection
If you are currently taking anticoagulant therapy, please inform our phlebotomist. An FTA card finger‑prick sample may be recommended in place of a venipuncture whole blood draw. Do not discontinue any prescribed medication without consulting your primary healthcare provider.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients actively on anticoagulant therapy – alternative sample types (FTA card) arranged after physician clearance.
- Emergency: Seek immediate medical care if the patient shows signs of increased intracranial pressure, new‑onset seizures, or rapidly progressive skull deformity.
Patient FAQ & Clinical Guidance
1. What is the MSX2 gene and its link to parietal foramina type 1?
Mutations in the MSX2 gene cause parietal foramina type 1, a congenital skull ossification defect detectable by NGS. These mutations disrupt normal bone formation in the parietal bones, leading to small openings that may close spontaneously or be associated with headaches, scalp defects, or developmental concerns. Genetic counseling clarifies the autosomal dominant inheritance pattern and recurrence risks for families.
2. How is the sample collected and what are the requirements?
Our VIP Mobile Phlebotomy service collects a standard whole blood sample (two EDTA tubes) at your home between 8 AM and 11 PM daily. Alternatively, an FTA card finger-prick sample can be used for patients with bleeding risks. A pre-collection genetic counseling session is recommended to obtain a detailed family pedigree and confirm test appropriateness. Collection is always preceded by a confirmation call.
3. What is the turnaround time and price?
The MSX2 gene NGS analysis is completed within 3–4 weeks from sample receipt. The price is 2,800 AED, inclusive of interpretation and a clinician-friendly report. Express reporting is available upon request. Insurance direct billing can be verified through our WhatsApp line at +971 54 548 8731.
4. Will this test replace imaging studies?
No. The genetic test identifies the molecular cause of parietal foramina but does not substitute for clinical evaluation or skull imaging (e.g., CT, X-ray). Radiological confirmation and correlation with the genetic finding are essential for a comprehensive diagnosis and management plan.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License Number 1143 and complies with all applicable UAE federal data protection and health information frameworks. All personal and genetic data is handled in accordance 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. Clinical testing safety and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | MSX2 Gene Parietal Foramina Type 1 Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Whole blood (EDTA) or FTA card finger-prick |
| Methodology Used | Next Generation Sequencing (NGS), full gene coverage |
| ICD-10-CM Code | Q75.8, Q75.0 |
| LOINC Code | 51966-2 |
| DHA Facility License & Address | License #1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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