Test Price
2,800 AED✅ Home Collection Available
TRPM6 Gene Hypomagnesemia Type 1 Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
Executive Summary: 99.9% Diagnostic Sensitivity with ISO Accredited Processing
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The TRPM6 Gene Hypomagnesemia Type 1 Genetic Test identifies pathogenic variants in the TRPM6 gene, the definitive molecular cause of primary familial hypomagnesemia with secondary hypocalcemia. This test enables precise diagnosis, guides magnesium and calcium therapy, and supports family screening for at-risk relatives.
| Feature | Our NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | High-coverage Next‑Generation Sequencing | Single‑gene Sanger (limited regions) |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks |
| Gene Coverage | Full coding region + splice sites | Selected exons only |
| Clinical Insight | Comprehensive mutation spectrum | May miss deep intronic variants |
| Price | 2800 AED | Similar / often higher with add‑ons |
Physician Insight & Safety Protocols
As a Consultant Medical Genetics, I emphasize that a positive TRPM6 mutation identifies the underlying genetic cause. Clinical correlation with serum magnesium and calcium levels is essential, and genetic counseling is recommended for family members. Do not adjust supplementation without consulting your specialist.
— Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Medication Advisory
Do not adjust or discontinue prescribed magnesium or calcium supplements without consulting your specialist. This test is a diagnostic tool and does not replace clinical management.
Safety & Exclusion Criteria
Eligibility Precautions
- Pregnancy without a specific medical indication.
- Minors (<18 years) without parental/legal guardian consent in accordance with UAE regulations.
- Severe acute illness that may compromise sample integrity.
Emergency Red Flags — Call 998 immediately:
- Unexplained seizures or tetany
- Severe muscle cramps with cardiac palpitations
- Sudden onset of cardiac arrhythmia
Patient FAQ & Clinical Guidance
1. What is the TRPM6 gene test used for?
The TRPM6 gene test detects mutations causing hereditary hypomagnesemia type 1, supporting diagnosis and management.
2. How fast can I get my TRPM6 test results?
Your confidential TRPM6 gene results are ready in 3-4 weeks through our secure online portal.
3. Will my UAE insurance cover this genetic test?
UAE insurers often cover TRPM6 testing when clinically indicated; we offer direct billing verification via WhatsApp.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance & Data Privacy
This test is performed 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 safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.
ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139). DHA Facility License: 1143.
Clinical & Logistical Metadata
| Test Name | TRPM6 Gene Hypomagnesemia Type 1 Genetic Test |
| Price (AED) | 2800 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral whole blood (EDTA tube) |
| Methodology Used | Next-Generation Sequencing (NGS) |
| ICD-10-CM Code | E83.42 |
| LOINC Code | 93257-0 |
| DHA Facility License & Address | License: 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians