SLC26A6 Gene Hyperoxaluria SLC26A6 Related NGS Genetic DNA Test
Introduction
The SLC26A6 Gene Hyperoxaluria SLC26A6 Related NGS Genetic DNA Test is a state-of-the-art diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze genetic predispositions to hyperoxaluria, a metabolic disorder that can lead to kidney stones and renal failure. Understanding your genetic makeup is crucial for early intervention and management of this condition.
What the Test Measures
This test specifically measures mutations in the SLC26A6 gene, which are linked to the development of hyperoxaluria. By identifying these mutations, healthcare providers can better assess the risk of developing related health issues.
Who Should Consider This Test
This test is particularly recommended for individuals who exhibit symptoms of hyperoxaluria or have a family history of metabolic disorders. Symptoms may include:
- Frequent kidney stones
- Recurrent urinary tract infections
- Family history of kidney disease
Benefits of Taking the Test
- Early detection of genetic predispositions to metabolic disorders.
- Informed decision-making regarding lifestyle and dietary adjustments.
- Guidance on family planning and potential risks for future generations.
Understanding Your Results
Results from the SLC26A6 Gene Hyperoxaluria NGS Genetic DNA Test will provide insights into your genetic risk factors. A genetic counselor can help interpret these results, discussing their implications for your health and family.
Test Name and Price
| Price Type | Price (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
We Are Here for You
With branches across major cities in Kenya, we offer convenient access to the SLC26A6 Gene Hyperoxaluria NGS Genetic DNA Test. Our services include home sample collection for your convenience.
Book Your Test Today!
Don’t wait to gain insights into your health. Contact us at +254711564616 to book your test or for more information!
