Is my genetic data protected?

Yes, your genetic information is fully compliant with UAE PDPL and encrypted. It is accessible only to authorised medical professionals.

Molecular Diagnostics → Glucocorticoid Deficiency

Results: 3–4 Weeks Sample: Whole Blood (EDTA) or FTA Card Blood Spot

Test Price

2,800 AED

✅ Home Collection Available

📋 Results in 3–4 Weeks

MC2R Gene Glucocorticoid Deficiency Type 1 Genetic Test in UAE

Q: What does the MC2R gene test detect and why is it important?

The MC2R gene test identifies pathogenic variants responsible for familial glucocorticoid deficiency type 1. This enables early intervention to prevent life-threatening adrenal crises.

Q: How is the test performed and what sample is required?

A simple blood draw (whole blood in EDTA) or a one-drop blood sample on an FTA card is required. Our DHA-licensed phlebotomists can collect the sample during a scheduled home visit.

Q: What does the 2800 AED price include?

The all-inclusive fee covers genetic counselling, home collection, NGS sequencing, and a final clinical report. We provide direct billing verification and pre-approval assistance via WhatsApp.

Q: How long does it take to get results?

The turnaround time is 3–4 weeks from the date the sample reaches our laboratory. You will receive a comprehensive report via email or patient portal.

Executive Summary & Core Metrics

Clinical Confidence, Zero Stress.

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Sequencing.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM – 11 PM).
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed genetic counsellors.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 (tap to chat).

Test Overview & Methodology

This genetic test analyzes the MC2R gene to diagnose familial glucocorticoid deficiency type 1, a rare inherited adrenal insufficiency that can lead to life-threatening hypoglycemia if undetected. Our DHA-compliant protocol delivers results in 3–4 weeks, empowering General Physicians, Endocrinologists, and Medical Geneticists with actionable genetic evidence.

Feature	Our MC2R NGS Test	Conventional Sanger Sequencing / Single-Gene Approach
Precision	99.9% Sensitivity & Specificity via NGS with full exon coverage	High accuracy but may miss deep intronic variants
Methodology	NGS (Next Generation Sequencing) – Clinically Validated	Sanger sequencing of coding regions only
Turnaround Time	3–4 Weeks	4–6 Weeks
Regulatory Compliance	Full UAE PDPL & DHA Guideline Adherence	May lack explicit UAE genetic data protection

Physician Insight & Safety Protocols

Clinical Note from Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA ID: 9294403:

"Every MC2R variant must be correlated with clinical cortisol levels and ACTH stimulation testing. This NGS test identifies pathogenic mutations, but the diagnosis of glucocorticoid deficiency type 1 requires biochemical confirmation. Genetic results alone do not replace endocrine evaluation."

Medication & Safety Advisory

Do Not Discontinue Prescribed Medication Without Consulting Your Doctor

Abrupt cessation of glucocorticoid therapy can precipitate an adrenal crisis. Always consult your endocrinologist before making changes to your medication regimen.

Exclusion Criteria for Home Collection

Acute respiratory distress or unstable vital signs.
Active febrile illness > 38.5°C.
Uncontrolled seizure disorder within past 24 hours.
Minors without legal guardian consent (per Federal Decree-Law No. 4 of 2016 on Medical Liability).

Emergency Red Flags – Seek Immediate Care

Sudden confusion, loss of consciousness, or severe lethargy.
Profound dehydration, vomiting, or diarrhea with inability to retain fluids.
Hypotension (systolic BP < 90 mmHg) or signs of shock.

Patient FAQ & Clinical Guidance

1. What does the MC2R gene test detect and why is it important for my child?

The MC2R gene test identifies pathogenic variants responsible for familial glucocorticoid deficiency type 1, enabling early intervention to prevent life-threatening adrenal crises. If your child has symptoms such as recurrent hypoglycemia, hyperpigmentation, or failure to thrive, this test can provide a definitive diagnosis.

2. How is the test performed and what sample is required?

We require a simple blood draw (whole blood in EDTA) or a one-drop blood sample on an FTA card. Our DHA-licensed phlebotomists can collect the sample during a scheduled home visit, ensuring minimal discomfort. The sample is then processed using Next Generation Sequencing at our accredited laboratory.

3. What does the 2800 AED price include and how do I use insurance?

The all-inclusive fee covers genetic counselling, home collection, NGS sequencing, and a final clinical report. We provide direct billing verification and pre-approval assistance via WhatsApp at +971 54 548 8731. Many insurance plans cover the test; contact us to check your eligibility.

4. How long does it take to get results?

The turnaround time is 3–4 weeks from the date the sample reaches our laboratory. You will receive a comprehensive report via email or patient portal, with a follow-up appointment scheduled with our genetic counsellor if needed.

UAE Regulatory & Data Privacy Adherence

Data Protection: Fully compliant with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL). Your genetic information is encrypted and accessible only to authorised medical professionals.
Health Data Handling: Adheres to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields for secure digital records and teleconsultation.
Consent & Liability: All collection and testing procedures follow Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring informed consent and patient safety.
Accreditations: Laboratory ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	MC2R Gene Glucocorticoid Deficiency Type 1 Genetic Test
Price (AED)	2,800 AED
Turnaround Time	3–4 Weeks
Sample Type / Matrix	Whole Blood (EDTA) or FTA Card Blood Spot
Methodology Used	Next Generation Sequencing (NGS) – Full Exon Coverage
ICD-10-CM Code	E27.49
LOINC Code	96521-6
DHA Facility License & Laboratory Address	License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE \| DNA Labs UAE

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Medically Reviewed by Dr. Lina Osama Zaki Quteineh

All content reviewed by qualified professionals for accuracy.

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ISMS 27001:2022

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All reports reviewed by DHA-Certified physicians