SLC12A3 Gene Gitelman Syndrome NGS Genetic DNA Test
The SLC12A3 Gene Gitelman Syndrome NGS Genetic DNA Test is a comprehensive genetic test designed to identify mutations in the SLC12A3 gene, which are responsible for Gitelman syndrome. This condition is characterized by electrolyte imbalances, leading to symptoms such as muscle weakness, fatigue, and low blood pressure. Understanding your genetic predisposition to this syndrome is crucial for effective management and treatment.
What the Test Measures
This test detects specific mutations in the SLC12A3 gene using Next-Generation Sequencing (NGS) technology. By analyzing the genetic material, healthcare providers can determine if a patient is at risk for developing Gitelman syndrome or if they are already affected by it.
Who Should Consider This Test?
Individuals who experience symptoms such as:
- Muscle cramps
- Fatigue
- Low blood pressure
- Increased thirst and urination
Additionally, those with a family history of Gitelman syndrome or related electrolyte disorders should consider this test.
Benefits of Taking the Test
- Identifies genetic mutations associated with Gitelman syndrome.
- Helps in understanding the underlying causes of symptoms.
- Guides treatment options and lifestyle changes.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SLC12A3 Gene Gitelman Syndrome NGS Genetic DNA Test will be available within 3 to 4 weeks. A genetic counseling session is recommended to help interpret the results, discuss their implications, and plan any necessary follow-up actions.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC12A3 Gene Gitelman Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
We have branches across major cities in Kenya, and we also offer home sample collection services for your convenience. To book the SLC12A3 Gene Gitelman Syndrome NGS Genetic DNA Test or for more information, please call or WhatsApp us at +254711564616.
