SLC12A5 Gene Bartter Syndrome NGS Genetic DNA Test
Introduction
The SLC12A5 Gene Bartter Syndrome NGS Genetic DNA Test is an advanced diagnostic test designed to identify mutations in the SLC12A5 gene, which are associated with Bartter syndrome. This condition is characterized by a group of rare kidney disorders that affect the body’s ability to reabsorb sodium, chloride, and potassium, leading to imbalances in electrolyte levels. Early detection through genetic testing is vital for managing symptoms and preventing complications.
What the Test Measures
This genetic test specifically measures the presence of mutations in the SLC12A5 gene. By utilizing Next Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the genetic material, allowing for accurate identification of genetic variations that may lead to Bartter syndrome.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Frequent dehydration
- Low blood pressure
- Muscle weakness
- Growth delays in children
Additionally, those with a family history of kidney disorders or electrolyte imbalances should consider this test to assess their genetic risk.
Benefits of Taking the Test
- Identifies genetic predispositions to Bartter syndrome.
- Enables informed health decisions and management strategies.
- Facilitates early intervention and treatment options.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SLC12A5 Gene Bartter Syndrome NGS Genetic DNA Test will indicate whether mutations are present. A genetic counselor will help interpret these results, explaining their implications for your health and any necessary lifestyle adjustments or treatments.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC12A5 Gene Bartter Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
The turnaround time for results is approximately 3 to 4 weeks. Samples can be collected via blood or extracted DNA, or even a single drop of blood on an FTA card. Prior to testing, a clinical history of the patient is required, along with a genetic counseling session to create a pedigree chart of family members affected by Bartter syndrome.
Branches and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu. To book the SLC12A5 Gene Bartter Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
