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Test Price

2,800 AED

✅ Home Collection Available

MECP2 Gene Duplication Syndrome (Lubs Type) Genetic Test in UAE

Executive Summary & Core Metrics

Executive Summary: Our laboratory delivers next-generation sequencing (NGS) for the MECP2 gene with a diagnostic sensitivity of 99.9%, adhering to ISO 9001:2015 standards and fully compliant with UAE 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. We ensure complete confidentiality of your genetic data, VIP mobile phlebotomy with temperature-controlled cold-chain home collection (daily 8 AM to 11 PM), and post-result tele-genetic counselling by our consultant medical geneticist.

Core Metrics: 2,800 AED · 3–4 weeks turnaround · NGS with CNV detection · ICD-10-CM Q99.8 · LOINC 82117-7 · DHA Facility License 1143 · ISO 9001:2015 Certified

Hospital-Grade Home Collection

VIP mobile phlebotomy & ISO-certified cold-chain transport, 8 AM – 11 PM, 7 days a week.

Direct Insurance Billing Verification

WhatsApp +971 54 548 8731 for instant confirmation of coverage under your UAE plan.

Test Overview & Methodology

The MECP2 Gene Duplication (Lubs Type) Test is a next-generation sequencing (NGS) analysis that detects copy-number variants and point mutations in the MECP2 gene on the X chromosome, the definitive cause of Lubs syndrome (X-linked syndromic intellectual disability). It provides unparalleled diagnostic clarity for neurologists assessing unexplained developmental delay, hypotonia, and recurrent infections in male patients.

Feature Our MECP2 NGS Test Common Single-Gene / MLPA Alternative
Precision Full gene sequencing + dosage analysis (CNV) Deletion/duplication only, misses point mutations
Methodology NGS (Illumina platform) with customized bioinformatics MLPA or Sanger sequencing limited to specific exons
Turnaround 3–4 weeks with DHA-compliant report 6–8 weeks commonly outside UAE accredited labs

Physician Insight & Safety Protocols

“As a Consultant Medical Genetics specialist, I view the MECP2 duplication test as a critical diagnostic anchor for Lubs syndrome, but it must always be interpreted alongside the child’s full clinical phenotype, developmental trajectory, and family pedigree. A positive finding confirms the genetic aetiology, yet it does not predict severity or progression in isolation. Our protocol mandates pre-test counselling so that families understand the implications for recurrence risk and anticipatory management, and post-test counselling to translate raw genomic data into a clear, actionable care roadmap.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403

Medication Advisory

Do not discontinue any prescribed anti-epileptic, neurodevelopmental, or respiratory medication without explicit instruction from your managing physician. Genetic test results complement, but do not replace, ongoing clinical management and therapeutic monitoring.

Exclusion Criteria & ER Red Flags

  • Acute febrile illness or untreated sepsis – collection deferred until resolved.
  • Imminent risk of self-harm or uncontrolled seizures – proceed directly to emergency department.
  • Known coagulopathy not managed – contact our clinical team for alternative sample type.

Patient FAQ & Clinical Guidance

1. What symptoms indicate a need for MECP2 duplication testing?

Early-onset hypotonia, severe intellectual disability, recurrent respiratory infections, and stereotypic hand movements in a male infant strongly suggest Lubs syndrome – our NGS test confirms the MECP2 duplication with high accuracy.

2. Is a fasting blood sample required for this genetic test?

No fasting is needed; a simple blood draw, dried blood spot (FTA card), or submitted extracted DNA suffices – our process accommodates all three sample types for convenience.

3. What UAE regulations protect my child’s genetic data?

Your data is protected under 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. We enforce strict parental consent protocols and encrypted storage for all genomic records.

4. How is the sample collected for this genetic test?

A standard peripheral blood draw is performed by our trained phlebotomist during a VIP home visit or at our Dubai Healthcare City facility. The sample is transported under temperature-controlled cold-chain to our ISO-accredited laboratory.

5. How long does it take to get results?

Turnaround time is 3–4 weeks from sample receipt. Your report includes a detailed clinical interpretation and a direct phone consultation with our consultant medical geneticist.

UAE Regulatory & Data Privacy Adherence

Data Privacy & Compliance Framework

Your genetic and personal data is processed in full 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. We implement encrypted storage, role-based access controls, and strict data minimization protocols. Clinical safety and patient consent procedures follow Federal Decree-Law No. 4 of 2016 on Medical Liability.

Our DHA-licensed facility (License No. 1143) at Dubai Healthcare City undergoes regular audit to maintain ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name MECP2 Gene Duplication Syndrome (Lubs Type) Genetic Test
Price (AED) 2,800 AED
Turnaround Time 3–4 weeks
Sample Type / Matrix Peripheral whole blood (EDTA) · Dried blood spot (FTA card) · Extracted DNA
Methodology Used Next-Generation Sequencing (NGS) with CNV detection
ICD-10-CM Code Q99.8, Z15.89, G93.89
LOINC Code 82117-7
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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All reports reviewed by DHA-Certified physicians