PDGFRB Gene Myeloproliferative disorder, chronic, with eosinophilia NGS Genetic Test
Also known as: Myeloproliferative disorder with eosinophilia, PDGFRB mutation disorder
PDGFRB Gene Myeloproliferative disorder, chronic, with eosinophilia NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) on Blood, Extracted DNA, or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To detect mutations in the PDGFRB gene for the diagnosis and management of myeloproliferative disorder with eosinophilia.
- Test Code
- 5606
- Price
- ₹20,000
- Sample Type
- Blood, Extracted DNA, or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- NGS (Next-Generation Sequencing)
Sample Collection
No special preparation required. Provide clinical history and undergo genetic counseling.
Method: Blood draw or FTA card collection
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist or FTA card used for collection.
Report Delivery
Apply pressure to the puncture site to stop bleeding. Resume normal activities.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the PDGFRB gene for the diagnosis and management of myeloproliferative disorder with eosinophilia.
How to Prepare
- Ensure proper identification
- Use sterile equipment
- Follow standard blood collection protocols
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This test is crucial for diagnosing PDGFRB-related myeloproliferative disorders and guiding treatment decisions for patients with chronic eosinophilia."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or insufficient sample
- Improper labeling
Understanding Your Results
Normal
No pathogenic mutations detected in the PDGFRB gene.
Abnormal
Pathogenic mutation detected, indicating a diagnosis of PDGFRB-related myeloproliferative disorder.
If experiencing symptoms of myeloproliferative disorder or for follow-up after abnormal test results.
Limitations
- ⚠Test only analyzes the PDGFRB gene; other genetic causes may not be detected
Risks & Considerations
- ●Minimal physical risk from blood draw
- ●Potential psychological impact of genetic results
Interfering Factors
- ●Sample quality or contamination may affect results
Frequently Asked Questions
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