Test Price
2,800 AEDโ Home Collection Available
CSF3R Gene Hereditary Neutrophilia NGS Diagnostic Test | Dubai Healthcare City
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance by Consultant Medical Genetics.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This diagnostic next-generation sequencing (NGS) test analyzes the entire coding region of the CSF3R gene for germline mutations associated with hereditary neutrophilia. Hereditary neutrophilia is a rare genetic condition characterized by persistently elevated neutrophil counts, splenomegaly, and an increased lifetime risk of myeloid malignancies such as chronic myelomonocytic leukemia (CMML) and acute myeloid leukemia (AML). Early molecular diagnosis enables targeted surveillance and proactive hematologic management.
Why Our Test Outperforms Standard Panels
| Feature | Our CSF3R NGS Test | Closest Alternative |
|---|---|---|
| Precision | Full gene sequencing with CNV detection, ACMG 2024 guidelines | Targeted mutation panel (common variants only) |
| Methodology | NGS on Illumina platform, verified by Sanger for all pathogenic calls | Sanger sequencing of selected exons |
| Turnaround | 3โ4 Weeks with dual-clinician interpretation | 4โ6 Weeks |
Physician Insight & Safety Protocols
"A positive CSF3R germline variant confirms the molecular diagnosis of hereditary neutrophilia, but results must be meticulously correlated with the patient's clinical phenotype, complete blood count (CBC) trajectory, and three-generation family pedigree. Genetic results alone are insufficient for therapeutic intervention; integration with a hematology consultation and longitudinal monitoring is mandatory. Comprehensive genetic counseling is essential for the patient and at-risk relatives."
โ Ms. Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication & Clinical Advisory
โ ๏ธ Important Clinical Safety Notice
This test is regulated under Federal Decree-Law No. 4 of 2016 on Medical Liability. Do not discontinue any prescribed hematologic or immunosuppressive therapy without consulting your managing physician. Abrupt cessation of treatment can lead to life-threatening complications. This test is an adjunct to clinical decision-making and does not replace comprehensive medical evaluation.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Individuals with an active acute infection, recent systemic illness, or blood transfusion within the past 4 weeks should defer testing to avoid confounding genetic results.
- Emergency Red Flags: If you experience unexplained fever, severe bone pain, easy bruising, or excessive bleeding while awaiting test results, seek immediate care at the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What is the clinical utility of CSF3R gene testing for neutrophilia?
This test definitively identifies germline CSF3R mutations that cause hereditary neutrophilia, enabling accurate risk stratification for myeloid malignancies such as CMML and AML. It allows for tailored surveillance strategies and informed family counseling.
2. How is the sample collected, and is home service available in the UAE?
A certified phlebotomist performs a simple blood draw at your home or office between 8 AM and 11 PM, adhering to strict temperature-controlled cold-chain protocols for specimen integrity.
3. Will my insurance cover this test and how is my genetic privacy ensured?
We verify direct billing with major UAE insurers. All genetic data is strictly protected under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and stored on encrypted UAE-based servers.
UAE Regulatory & Data Privacy Adherence
Data Privacy & Health Information Governance
DNA Labs UAE strictly 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 genetic data is encrypted, stored on UAE-based servers, and processed under strict confidentiality agreements. Your genomic information is your property; we do not share it with third parties without your explicit written consent.
Clinical & Logistical Metadata
| Test Name | CSF3R Gene Hereditary Neutrophilia NGS Diagnostic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (2 mL in EDTA tube) |
| Methodology Used | Next-Generation Sequencing (NGS) on Illumina Platform, Sanger Confirmation |
| ICD-10-CM Code | D72.0 |
| LOINC Code | 94362-4 |
| DHA Facility License & Laboratory Address | 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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