FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic Test
FGF23 Gene Hypophosphatemic rickets, autosomal dominant NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or 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 identify pathogenic mutations in the FGF23 gene that cause autosomal dominant hypophosphatemic rickets, aiding in accurate diagnosis and personalized treatment planning.
- Test Code
- 2126
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- Yes
- Method
- NGS Technology
Sample Collection
Patient should provide detailed clinical history of symptoms and family history of hypophosphatemic rickets. A genetic counseling session is recommended to draw a pedigree chart.
Laboratory Analysis
Your sample is analyzed using NGS Technology in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic mutations in the FGF23 gene that cause autosomal dominant hypophosphatemic rickets, aiding in accurate diagnosis and personalized treatment planning.
How to Prepare
- Blood sample: Standard venipuncture procedure.
- FTA Card: One drop of blood on FTA card as per instructions.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Early genetic testing for FGF23 mutations can guide treatment for hypophosphatemic rickets, preventing bone deformities and improving quality of life."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of FGF23 gene-related hypophosphatemic rickets.
No pathogenic variant detected
Reduces likelihood of FGF23 gene mutation; consider other genetic or environmental factors.
If you experience symptoms such as bone pain, deformities, or tooth problems, or have a family history of hypophosphatemic rickets, consult a healthcare provider for genetic testing and counseling.
Frequently Asked Questions
What is FGF23 Gene Hypophosphatemic Rickets?
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