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Test Price

1,400 AED

✅ Home Collection Available

AML Panel Deletion/Duplication Detection in UAE | 1400 AED | DHA Licensed

Executive Summary & Core Metrics

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

Premium Logistics: 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

This test identifies gene deletions and duplications in AML-associated genes using Multiplex Ligation-dependent Probe Amplification (MLPA), providing critical prognostic and therapeutic insights.

Feature Our MLPA Panel FISH/Karyotyping
Resolution Single-exon deletions/duplications Large structural abnormalities (>5 Mb)
Method Advanced MLPA, quantitative Fluorescence in situ hybridization
Turnaround Time 7–10 days Up to 14 days

Physician Insight & Safety Protocols

"As a Consultant Medical Genetics, I understand that precision genetic profiling is crucial for AML management. Our MLPA panel provides high-resolution deletion/duplication analysis to guide targeted therapy. Please use these results in consultation with your oncologist. Do not discontinue prescribed medication without professional advice."

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

Important Safety Advisory

Clinical Guidance

This test should only be performed under the direction of a qualified hematologist/oncologist. Results must be interpreted alongside clinical findings and other diagnostic tests. Do not use as a standalone diagnostic tool.

Exclusion Criteria & ER Red Flags

Exclusion Criteria

  • Current active chemotherapy or radiation therapy (wait 2 weeks post-cycle).
  • Bone marrow transplant within last 3 months.
  • Uncontrolled acute infections or febrile neutropenia.
  • Seek emergency care if: severe bone pain, fever >38.5°C, uncontrolled bleeding, or new neurological symptoms.

Patient FAQ & Clinical Guidance

1. What does an AML gene deletion/duplication test detect and why is it ordered?

An AML gene deletion/duplication using MLPA identifies specific DNA segment losses or gains in leukemia cells to guide prognosis and targeted therapy.

2. How is the bone marrow or blood sample collected for AML panel testing?

A bone marrow aspirate or peripheral blood sample is collected by a trained phlebotomist using strict aseptic technique and transported immediately in a cold chain. As this test requires an invasive procedure, collection is strictly performed within a hospital setting.

3. What is the turnaround time for AML deletion/duplication panel results?

Standard turnaround time is 7 to 10 days, enabling timely, evidence-based clinical decision-making for AML patients.

UAE Regulatory & Data Privacy Adherence

Data Protection: This service complies 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. Patient consent and clinical safety adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Accreditations: ISO 9001:2015 Cert: INT/EGQ/2509DA/3139. DHA facility license: 1143.

Clinical & Logistical Metadata

Test Name AML Panel Deletion/Duplication Detection
Price (AED) 1400 AED
Turnaround Time 7–10 days
Sample Type / Matrix Bone Marrow Aspirate or Peripheral Blood (Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.)
Methodology Used Multiplex Ligation-dependent Probe Amplification (MLPA)
ICD-10-CM Code C92.00
LOINC Code 93385-0
DHA Facility License & Laboratory Address DHA Facility License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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