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Test Price

3,200 AED

✅ Home Collection Available

Acute Myeloid Leukemia (AML) Cytogenetics Panel in UAE | 3,200 AED | DNA Labs UAE

Executive Summary & Core Metrics

DNA Labs UAE | DHA Facility License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

Our ISO 9001:2015‑certified laboratory (Cert: INT/EGQ/2509DA/3139) delivers an AML‑dedicated cytogenetics panel with 99.9% diagnostic sensitivity using dual‑platform fluorescence in-situ hybridization (FISH) and conventional G‑banded karyotyping. We strictly comply 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. Clinical safety and consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Sample collection logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. Cold‑chain transport and 4‑working‑day reporting apply. Telephonic post‑test clinical guidance and direct billing verification is available via WhatsApp +971 54 548 8731.

Lead Clinical Oversight: Mr. Prabhakar Reddy Kalathoor | Specialist Diagnostic Radiology | DHA Registration ID: 61713011

Test Overview & Methodology

Using gold‑standard fluorescence in‑situ hybridization (FISH) and G‑banded karyotyping on peripheral blood and bone marrow, this panel detects recurrent chromosomal aberrations that define AML subtypes, guide risk‑adapted therapy, and predict clinical outcome. The integrated dual-platform approach detects cryptic rearrangements and complex karyotypes that are often missed by FISH-only assays.

Comprehensive Comparison: Our Panel vs. Standard FISH‑Only Assay

Parameter Our AML Cytogenetics Panel Standard FISH‑Only Assay
Methodology FISH + Conventional Karyotyping (G‑banding) FISH alone (targeted probes)
Diagnostic Yield 99.9% sensitivity; detects cryptic rearrangements & complex karyotypes Limited to pre‑specified loci; may miss balanced translocations & ploidy changes
Turnaround Time Report in 4 working days Often 7–10 days due to sequential testing
Pre‑Test Requirement Form 17 mandatory; cold‑chain maintained Variable paperwork
ISO 9001:2015 Accreditation Yes (Cert: INT/EGQ/2509DA/3139) Not always guaranteed

Physician Insight & Safety Protocols

Mr. Prabhakar Reddy Kalathoor (DHA Registration ID: 61713011): “The AML cytogenetics panel is the cornerstone of prognostication; it distinguishes between favorable, intermediate, and adverse risk groups. Results must always be integrated with blast morphology and molecular markers for a definitive clinical picture. Any abnormal finding should prompt an immediate oncology consultation to tailor targeted therapies and avoid treatment delays.”

Medication Warning & Safety

Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

  • Contraindicated in patients with severe uncorrected coagulopathy (bleeding risk from bone marrow aspiration).
  • Not suitable for patients unable to give informed consent. Minors require guardian consent as stipulated by Federal Decree-Law No. 4 of 2016 on Medical Liability.
  • If the patient develops sudden fever, uncontrolled bleeding, respiratory distress, or altered mental status (possible leukostasis), seek emergency care immediately – do not wait for cytogenetic results.
  • Ensure the mandatory Chromosome and FISH Analysis Requisition Form (Form 17) is fully completed to avoid sample rejection.

Patient FAQ & Clinical Guidance

1. What does the AML Cytogenetics Panel detect?

A: This panel identifies specific chromosome abnormalities like translocations t(8;21), inversion inv(16), or complex karyotypes that are critical for classifying AML subtypes and predicting disease aggressiveness. Results guide whether standard chemotherapy, targeted agents, or bone marrow transplantation is indicated.

2. How should I prepare for the blood and bone marrow collection?

A: No fasting is required, but you must complete the Chromosome and FISH Analysis Requisition Form (Form 17) and inform your physician about all anticoagulants. The collection is performed by a specialist using sterile sodium heparin tubes, and the samples must never be frozen.

3. When will I receive my AML cytogenetics results?

A: Your comprehensive report is typically delivered within 4 working days from sample receipt, complete with interpretative comments and telephonic clinical guidance upon request. Urgent preliminary FISH results can be communicated earlier through your referring physician.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE operates in full compliance with the 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. All patient data is encrypted, access-controlled, and handled under strict confidentiality agreements. Clinical safety and consent procedures further adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name Acute Myeloid Leukemia (AML) Cytogenetics Panel
Price (AED) 3,200 AED
Turnaround Time 4 working days
Sample Type / Matrix Peripheral Whole Blood & Bone Marrow
(Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.)
Methodology Used FISH + Conventional Karyotyping (G‑banding)
ICD-10-CM Code C92.0 (Acute myeloid leukemia, not otherwise specified)
LOINC Code 91836-7 (Acute myeloid leukemia cytogenetics panel)
DHA Facility License & Address DHA License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

UAE Licensed Facility: DNA Labs UAE | DHA Facility License Number: 1143

Physical Address: Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

Home Collection: Not available for this test (hospital only) | Support & Insurance Billing: WhatsApp +971 54 548 8731

Strictly compliant with Federal Decree-Law No. 45 of 2021 (PDPL), Federal Law No. 2 of 2019, and Federal Decree-Law No. 4 of 2016.

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