Test Price
2,800 AED✅ Home Collection Available
MNX1 Gene Currarino Syndrome Genetic Test in UAE – 2,800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance Direct Billing Verification: Via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This advanced NGS test analyzes the complete coding region of the MNX1 gene to detect mutations causing Currarino syndrome, a rare dysmorphology disorder. The test delivers a comprehensive genetic profile essential for early pediatric surgical planning and familial risk assessment.
| Feature | Our Test (NGS) | Closest Alternative (Sanger) |
|---|---|---|
| Precision | Detects >99% of pathogenic variants | ~95% for single exon events |
| Method | Next Generation Sequencing (LC‑MS/MS‑assisted) | Sanger Sequencing |
| Turnaround Time | 3 to 4 Weeks | 5 to 8 Weeks |
Physician Insight & Safety Protocols
“This test must be interpreted in the full clinical context of anorectal malformations, sacral defects, and presacral masses. I strongly advise pre‑ and post‑test genetic counseling to correlate molecular findings with surgical and developmental outcomes. Your child’s care team will explain every result in a way that empowers informed decisions.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory Notes
Do not discontinue any prescribed medication without consulting your doctor.
Exclusion Criteria & ER Red Flags
- Inability to provide a clinical history of Currarino triad features (sacral defect, anal stenosis, presacral mass).
- Active febrile illness or systemic infection requiring immediate care.
- Severe coagulopathy that prevents safe venipuncture (use FTA card in such cases).
- Go to ER immediately if: Signs of bowel obstruction, sudden neurological deficits in lower limbs, or acute urinary retention develop during the testing period.
Patient FAQ & Clinical Guidance
1. What does a positive MNX1 result mean for my child’s surgery planning?
A pathogenic MNX1 variant confirms a genetic diagnosis of Currarino syndrome, enabling precise, staged surgical interventions by a multidisciplinary team that includes pediatric surgeons and neurosurgeons.
2. How do I prepare my child for the sample collection?
A pediatric genetic counselor will schedule a pre‑test consultation to draw a pedigree chart and explain the minimal requirements—either a small blood draw, a single drop on an FTA card, or extracted DNA submitted with a clinical history form.
3. Is home collection available for this genetic test in the UAE?
Yes, our ISO‑certified phlebotomy team provides hospital‑grade home collection between 8 AM and 11 PM daily, with direct billing verification through WhatsApp at +971 54 548 8731.
UAE Regulatory & Data Privacy Adherence
Data Protection: All personal and genetic data is handled in strict compliance 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.
Medical Liability: Clinical testing safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | MNX1 Gene Currarino Syndrome Sequencing |
| Price (AED) | 2,800 |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Whole Blood, Extracted DNA, or FTA Card Blood Spot |
| Methodology Used | Next Generation Sequencing (NGS) |
| ICD-10-CM Code | Q87.8 |
| LOINC Code | 21639-0 |
| DHA Facility License & Address | License No: 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