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Test Price

2,800 AED

✅ Home Collection Available

MECP2 Gene (Neonatal Severe Encephalopathy) Genetic Test in UAE | 2800 AED

Executive Summary & Core Metrics

✅ 99.9% Diagnostic Sensitivity – ISO 9001:2015 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 for result interpretation.

Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.

Test Overview & Methodology

The MECP2 Gene (Neonatal Severe Encephalopathy) Genetic Test is a next-generation sequencing (NGS) assay that screens the entire coding region of the MECP2 gene for pathogenic variants linked to severe early-onset encephalopathy and related neurodevelopmental disorders. This definitive molecular diagnosis supports targeted clinical management for affected neonates.

Feature Our Test (MECP2 NGS) Closest Alternative
Precision Full gene coverage, >99.9% analytical sensitivity Targeted mutation panels – limited variants
Methodology Next Generation Sequencing (NGS), LC‑MS/MS validated Sanger sequencing / fragment analysis
Speed 3–4 Weeks (comprehensive report) 4–6 Weeks for equivalent depth
Clinical Fit Neonatal Encephalopathy, Rett/Atypical Rett, MECP2 Duplication Usually limited to known familial mutations

Physician Insight & Safety Protocols

“The MECP2 gene test provides essential molecular information for diagnosing severe neonatal encephalopathy. However, it must be interpreted alongside detailed clinical findings and family history. A consultation with a genetics specialist is strongly advised.”

— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)

Safety Advisory

⚠️ Medication Warning

Do not discontinue prescribed medication without consulting your doctor. This test does not replace ongoing clinical care.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: Inability to provide a blood or FTA card sample; severely unstable neonate where phlebotomy is contraindicated.
  • ER Red Flags: Sudden deterioration of consciousness, apnea, or seizures after sample collection – seek immediate emergency care.
  • Minors: Sample collection from minors requires legal guardian consent in compliance with UAE law.

Patient FAQ & Clinical Guidance

1. What is the MECP2 gene test for neonatal severe encephalopathy?

It is a complete sequencing of the MECP2 gene to identify pathogenic variants causing severe brain dysfunction in newborns – yielding a definitive diagnosis in just 3–4 weeks.

2. How is the sample collected for this test in the UAE?

Sample collection is performed via a painless blood draw or a simple drop on an FTA card, handled by certified phlebotomists during a hospital-grade home visit.

3. What do the results mean and how long does it take?

Results detail the genetic variant found, its clinical significance, and recurrence risk – delivered in a comprehensive report within 3 to 4 weeks, followed by a post-test consultation.

UAE Regulatory & Data Privacy Adherence

  • Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – All genomic data encrypted and stored on-shore.
  • Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – Ensures secure handling of health data.
  • Federal Decree-Law No. 4 of 2016 on Medical Liability – Clinical testing safety and patient consent guidelines adhered to.
  • ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) – Quality management system for diagnostic accuracy.

Clinical & Logistical Metadata

Test Name MECP2 Gene (Neonatal Severe Encephalopathy) Genetic Test
Price (AED) 2,800
Turnaround Time 3 – 4 Weeks
Sample Type / Matrix Peripheral Whole Blood or Dried Blood Spot (FTA Card)
Methodology Used Next Generation Sequencing (NGS)
ICD-10-CM Code G93.4
LOINC Code 95162-5
DHA Facility License & Laboratory Address DHA License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE

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