Test Price
2,800 AED✅ Home Collection Available
GCM2 Gene Familial Isolated Hypoparathyroidism Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
- Diagnostic Accuracy: 99.9% analytical sensitivity achieved via ISO 9001:2015 accredited Next-Generation Sequencing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily 8 AM to 11 PM – no clinic visit required.
- Clinical Guidance: Telephonic post-test genetic counselling by DHA-licensed specialists for result interpretation and family planning.
- Insurance Support: Direct billing verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The GCM2 Gene Familial Isolated Hypoparathyroidism Test uses Next-Generation Sequencing (NGS) to detect pathogenic variants in the GCM2 gene. This test confirms the genetic basis of isolated hypoparathyroidism, guiding endocrinology management and family planning decisions. Analysis is performed on peripheral whole blood with high-coverage sequencing aligned to current ACMG standards.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision | High-coverage NGS >99.9% analytical sensitivity | Lower resolution single-gene Sanger sequencing |
| Method | Next-Generation Sequencing (ACMG-aligned) | Conventional Sanger sequencing of selected exons |
| Speed | Results in 3–4 Weeks | Typically 4–6 weeks |
Test Prerequisites: Genetic counselling session and pedigree chart of family members affected by GCM2-related hypoparathyroidism are strongly recommended prior to sample collection.
Physician Insight & Safety Protocols
“A positive GCM2 finding must be correlated with clinical calcium levels and family history. Genetic results empower precise management but never replace regular endocrinology follow-up. I urge all patients to view this test as a step toward informed care, not a final verdict.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics | DHA Registration ID: 9294403
Medication Advisory
Do not discontinue prescribed calcium, vitamin D, or any endocrine medications without consulting your supervising physician. Genetic results do not grant authority to alter your treatment plan.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Individuals without a consenting legal guardian if under 18, active febrile illness, or inability to provide the required blood sample.
- Emergency Red Flags: Sudden muscle cramps, seizures, severe tingling around the mouth, or cardiac palpitations require immediate emergency care — these may indicate severe hypocalcemia unrelated to the testing process.
Patient FAQ & Clinical Guidance
1. How does the GCM2 NGS test differ from routine calcium blood tests?
This genetic test identifies the root cause at the DNA level, while calcium labs only measure current mineral levels. The result provides lifelong guidance for endocrine management and family screening.
2. Is home collection safe and reliable for a genetic test?
Yes, our VIP mobile phlebotomy service uses ISO-certified temperature-controlled cold-chain transport to preserve DNA integrity completely from your location to the laboratory.
3. What should I do if the result shows a GCM2 mutation?
Book a telephonic interpretation session with our genetics team to translate findings into your personalized care plan and discuss implications for at-risk family members.
UAE Regulatory & Data Privacy Adherence
All genetic testing and patient data handling at DNA Labs UAE comply 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 procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your genetic data is encrypted, access-controlled, and never shared without explicit written consent.
Clinical & Logistical Metadata
| Test Name | GCM2 Gene Familial Isolated Hypoparathyroidism Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (VIP Mobile Phlebotomy & Cold-Chain Home Collection Available) |
| Methodology Used | Next-Generation Sequencing (NGS) – High-Coverage, ACMG-Aligned |
| ICD-10-CM Code | E20.8 |
| LOINC Code | 79219-2 |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE |
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