Test Price
2,800 AED✅ Home Collection Available
STAMBP Gene Microcephaly‑Capillary Malformation Syndrome NGS Test in UAE | 2800 AED | DNA Labs UAE
Executive Summary & Core Metrics
Clinical Excellence & Trust Parameters
- 99.9% SENSITIVITY ISO‑accredited NGS processing ensures unparalleled diagnostic precision.
- VIP HOME COLLECTION Temperature‑controlled cold‑chain mobile phlebotomy available daily from 8 AM to 11 PM across the UAE.
- CLINICAL GUIDANCE Post‑test result interpretation via teleconsultation by a DHA‑licensed Consultant in Medical Genetics.
- INSURANCE SUPPORT Direct billing verification is available via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The STAMBP gene NGS test sequences all coding regions to detect pathogenic variants causing microcephaly‑capillary malformation syndrome – a rare neurovascular disorder combining microcephaly, capillary malformations, and systemic anomalies. State‑of‑the‑art Next‑Generation Sequencing with bi‑directional Sanger confirmation delivers a definitive molecular diagnosis in 3–4 weeks.
| Feature | Our STAMBP NGS Test | Closest Alternative (Single‑gene Sanger) |
|---|---|---|
| Molecular Coverage | Full coding exons + splice junctions | Selected hotspot regions only |
| Sensitivity | >99.9% (analytical sensitivity) | ~95% (may miss novel variants) |
| Turnaround Time | 3–4 weeks with clinical report | ~6–8 weeks |
Physician Insight & Safety Protocols
Clinical Advisory & Medication Stability
⚠️ Do not discontinue any prescribed medication without consulting your doctor.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Recent allogeneic blood transfusion or stem cell transplant (within 3 months) may produce chimeric DNA interfering with germline analysis.
- Exclusion: Inability to provide sufficient DNA sample or lack of informed consent.
- Emergency Red Flags: New‑onset seizures, sudden severe headache, loss of consciousness, rapid developmental regression, or acute neurological deterioration – seek immediate emergency care.
Patient FAQ & Clinical Guidance
1. What does the STAMBP gene test detect?
The STAMBP NGS test sequences the entire coding region to identify pathogenic mutations causing microcephaly‑capillary malformation syndrome, a rare neurovascular disorder with brain and skin abnormalities. This molecular diagnosis aids in confirming clinical suspicion, guides management, and enables family genetic counseling. Results include variant classification according to ACMG guidelines.
2. How is the sample collected?
A blood sample is drawn through gentle venipuncture, or a dried blood spot on an FTA card or saliva specimen can be collected. VIP mobile phlebotomy with temperature‑controlled cold‑chain logistics is available across the UAE from 8 AM to 11 PM. The collection process takes only minutes and is performed by certified phlebotomists. No special preparation such as fasting is required.
3. When will I receive my results?
Results are typically ready within 3 to 4 weeks from sample receipt, accompanied by a detailed clinical report including variant interpretation and family guidance. The comprehensive report is reviewed by a molecular geneticist and can be discussed with your referring physician during a teleconsultation.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License No. 1143 and strictly 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. All genetic testing requires explicit informed consent as mandated by Federal Decree-Law No. 4 of 2016 on Medical Liability. Our laboratory holds ISO 9001:2015 certification. Genetic counseling is strongly recommended before and after testing. For insurance billing inquiries, contact us via WhatsApp at +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | STAMBP Gene Microcephaly‑Capillary Malformation Syndrome NGS Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 weeks |
| Sample Type / Matrix | Whole Blood (EDTA), Dried Blood Spot (FTA Card), or Saliva (Oragene DNA Kit) |
| Methodology Used | Next‑Generation Sequencing (NGS) with bidirectional Sanger confirmation |
| ICD-10-CM Code | Q87.2 (Congenital malformation syndromes predominantly involving limbs) |
| LOINC Code | 92868-0 (STAMBP gene targeted mutation analysis in Blood or Tissue by NGS) |
| DHA Facility License & Lab Address | 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