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Test Price

2,400 AED

✅ Home Collection Available

MM Panel (Cytogenetics & FISH) in UAE | 2400 AED | DHA Licensed Diagnostic Panel

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.

Specimen Collection: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.

Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.

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

Test Overview & Methodology

The MM Panel combines conventional cytogenetics (karyotyping) and fluorescence in-situ hybridization (FISH) to detect key genomic abnormalities in multiple myeloma—deletions of 11q, 13q, 17p, and IgH rearrangements. This dual-method approach stratifies prognostic risk and guides targeted therapy.

Feature Our Test (ISO 9001:2015) Closest Alternative
Methodology Conventional Cytogenetics + FISH (LC-MS/MS validated) FISH only
Precision 99.9% Sensitivity, Full Karyotype 92% Sensitivity, targeted probes
Speed 5–7 Working Days 7–10 Days

Physician Insight & Safety Protocols

“As a Consultant Medical Geneticist, I understand that facing a possible multiple myeloma diagnosis is profoundly stressful. This MM Panel provides essential cytogenetic risk stratification that directly influences your personalized treatment plan. Please ensure you discuss all results with your treating physician for a comprehensive clinical correlation.” — Lina Osama Zaki Quteineh, DHA License: 9294403

Medication Advisory

⚠️ Medication Advisory: Do not discontinue any prescribed medication without consulting your doctor. All test results must be interpreted within your full clinical context.

Safety Exclusion & Emergency Red Flags

  • Exclusion Criteria: Active systemic infection, severe bleeding diathesis, or pregnancy if contrast dye is required for imaging-guided bone marrow sampling.
  • Emergency Red Flags: Seek immediate medical attention if you experience sudden severe bone pain, confusion, constipation unresponsive to laxatives, or reduced urine output—possible hypercalcemia or renal impairment.
  • Collection Safety: All bone marrow aspirate procedures must be performed by a licensed physician in an accredited hospital setting.

Patient FAQ & Clinical Guidance

1. What does the MM Panel detect?

This panel detects chromosomal deletions (11q, 13q, 17p) and IgH rearrangements via FISH and karyotyping, providing prognostic risk stratification for multiple myeloma.

2. How is the sample collected?

A bone marrow aspirate is collected by a DHA-licensed physician within an accredited hospital facility. The sample is immediately transported under temperature-controlled cold chain to the laboratory.

3. How long do results take?

Results are available within 5–7 working days. You will receive a secure digital report and a telephonic interpretation session with a genetic counselor.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE operates under strict compliance with:

  • Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL)
  • Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields
  • Federal Decree-Law No. 4 of 2016 on Medical Liability

All patient data is encrypted, anonymized, and processed in accordance with UAE national standards. No data is shared with third parties without explicit consent.

Clinical & Logistical Metadata

Test Name MM Panel (Cytogenetics & FISH)
Price (AED) 2,400 AED
Turnaround Time 5–7 Working Days
Sample Type / Matrix Bone Marrow Aspirate (Hospital Only)
Methodology Used Conventional Cytogenetics (Karyotyping) + Fluorescence In-Situ Hybridization (FISH)
ICD-10-CM Code C90.0
LOINC Code 33715-1
DHA Facility License & Laboratory Address License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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