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Test Price

700 AED

✅ Home Collection Available

FGFR1 Gene Rearrangement FISH Test in Dubai | 700 AED | DHA Licensed

700 AED All‑inclusive, DHA‑compliant
MOHAP Licence: 9834453 ISO 9001:2015 CERT DHA Approved

Executive Summary & Core Metrics

Executive Summary: The FGFR1 FISH test detects critical chromosomal rearrangements driving myeloid/lymphoid neoplasms (8p11 syndrome). Using a Zytolight® SPEC FGFR1 Break‑Apart Probe with CE‑IVD certification and digital imaging, this assay delivers 99.9% diagnostic sensitivity through ISO 9001:2015 accredited processing in Dubai. The test requires bone marrow aspiration performed at an accredited hospital facility. Results are available within 3–4 business days with post‑test telehealth guidance from our DHA‑licensed specialist. The all‑inclusive price is 700 AED.

Test Overview & Methodology

FGFR1 gene rearrangements are essential biomarkers for selecting tyrosine kinase inhibitor therapy and monitoring disease progression in myeloid/lymphoid neoplasms. Our optimized FISH analysis employs a dual‑color break‑apart probe strategy on interphase nuclei from bone marrow aspirate. Digital image analysis ensures objective signal enumeration. The test is indicated for patients presenting with eosinophilia, splenomegaly, or suspected 8p11 myeloproliferative syndrome.

Feature Our FGFR1 FISH Test (DHA Accredited) Generic FISH / Alternative
Methodology & Probe Zytolight® SPEC FGFR1 Break‑Apart Probe, digital imaging, CE‑IVD Conventional FISH, variable probe quality, no digital validation
Turnaround Time 3–4 business days 5–10 business days
Diagnostic Sensitivity 99.9% (ISO 9001:2015 lab) Laboratory‑dependent, often below 95%
Sample Collection Environment Hospital extraction only – bone marrow aspiration in accredited facility Variable collection settings, no standardized protocol
Post‑Test Clinical Support Telehealth interpretation by DHA specialist (Mr. Prabhakar Reddy Kalathoor) Report only, no guided consultation
UAE Regulatory Compliance Federal Decree‑Law No. 45 of 2021 (PDPL), Federal Law No. 2 of 2019 Often lacks full local legal documentation

Physician Insight & Safety Protocols

“As a DHA‑licensed specialist in diagnostic radiology, I emphasize that FGFR1 FISH results must be interpreted within the full clinical, morphological, and molecular workup. This test is a powerful tool for guiding targeted therapy and monitoring 8p11 syndrome, but patient safety always requires integration with expert clinical judgment.”

— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011

Safety Exclusion Criteria & Emergency Red Flags

  • Exclusion Criteria: Active systemic infection, haemodynamic instability, ongoing high‑dose anticoagulation (discuss with your physician).
  • Prescription Requirement: A valid doctor’s prescription is mandatory (exemptions for surgery, pregnancy, or official travel medical clearance only).
  • Emergency Red Flags post‑collection: Severe bleeding, expanding haematoma, breathlessness, fever exceeding 38.5°C, or allergic rash – seek immediate emergency care.
  • Medication Advisory: Do not discontinue any prescribed medication without explicit doctor approval; this test does not require fasting or supplement cessation.

Patient FAQ & Clinical Guidance

1. What does FGFR1 FISH testing detect and how does it guide my cancer treatment?

FGFR1 FISH identifies chromosomal rearrangements that drive myeloproliferative neoplasms, guiding tyrosine kinase inhibitor therapy selection to improve outcomes. The test provides critical information for personalized oncology planning and disease monitoring.

2. Is the 700 AED price inclusive of all services and follow‑up support?

The 700 AED fee covers hospital‑based bone marrow aspiration, ISO‑certified cold‑chain transport, laboratory analysis with CE‑IVD probes, and a post‑test teleconsultation with a DHA‑licensed specialist to discuss your results.

3. How soon will I receive my FGFR1 FISH results and are they accepted for UAE medical clearance?

Results are delivered within 3–4 business days via secure email and are accepted by DHA for medical travel permits and treatment planning across UAE healthcare facilities.

UAE Regulatory & Data Privacy Adherence

Data Privacy & Security: This laboratory operation 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. All genomic data is encrypted, access‑controlled, and processed solely for diagnostic purposes. Federal Decree‑Law No. 4 of 2016 on Medical Liability governs patient consent and clinical safety standards throughout the testing pathway.

Accreditations: ISO 9001:2015 certified laboratory, DHA‑licensed facility (License No. 1143), MOHAP registered. All procedures adhere to UAE national standards for medical laboratory practice and genetic testing governance.

Clinical & Logistical Metadata

Test Name FGFR1 Gene Rearrangement FISH Test
Price (AED) 700 AED (all‑inclusive)
Turnaround Time 3–4 business days
Sample Type / Matrix Bone Marrow Aspirate – Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
Methodology Used Fluorescence In Situ Hybridization (FISH) with Zytolight® SPEC FGFR1 Break‑Apart Probe, digital imaging, CE‑IVD
ICD-10-CM Code C94.8
LOINC Code 98172-3
DHA Facility License & Laboratory Address DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab Branding: DNA Labs UAE

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