SLC9A3R1 Gene Nephrolithiasis Osteoporosis Hypophosphatemic Type 2 NGS Genetic DNA Test
Introduction
The SLC9A3R1 Gene Nephrolithiasis Osteoporosis Hypophosphatemic Type 2 NGS Genetic DNA Test is a cutting-edge diagnostic tool that helps in identifying genetic predispositions to nephrolithiasis (kidney stones) and osteoporosis (bone density loss). This test utilizes Next Generation Sequencing (NGS) technology to analyze the SLC9A3R1 gene, which is crucial in understanding these conditions.
What the Test Measures
This test specifically measures variations in the SLC9A3R1 gene that may contribute to the development of nephrolithiasis and osteoporosis. By detecting these genetic markers, healthcare providers can better assess an individual’s risk and tailor preventive measures accordingly.
Who Should Consider This Test
- Individuals with a family history of nephrolithiasis or osteoporosis.
- Patients experiencing symptoms such as recurrent kidney stones or unexplained bone fractures.
- Those with risk factors including metabolic disorders or chronic kidney disease.
Benefits of Taking the Test
- Identifies genetic risks that may not be apparent through standard clinical assessments.
- Enables proactive management and personalized treatment plans.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SLC9A3R1 Gene Nephrolithiasis Osteoporosis Hypophosphatemic Type 2 NGS Genetic DNA Test will indicate whether any genetic variations are present. A healthcare provider will help interpret these results, guiding you on the next steps based on your genetic profile.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Book Your Test Today!
We have branches across Kenya, making it convenient for you to access our services. For your convenience, we also offer home sample collection. To book the SLC9A3R1 Gene Nephrolithiasis Osteoporosis Hypophosphatemic Type 2 NGS Genetic DNA Test, call or WhatsApp us at +254711564616.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the SLC9A3R1 gene.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Hepatology, Nephrology, Endocrinology Disorders
