SLC12A2 Gene Bartter Syndrome NGS Genetic DNA Test
Introduction to the Test
The SLC12A2 Gene Bartter Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze the SLC12A2 gene. This gene plays a vital role in kidney function, and mutations can lead to Bartter syndrome, a rare genetic disorder characterized by imbalances in electrolytes and fluids. Understanding your genetic makeup is essential for early diagnosis and management of potential health issues.
What the Test Measures
This test specifically measures mutations in the SLC12A2 gene, which can result in various forms of Bartter syndrome. By identifying these mutations, healthcare providers can better understand an individual’s risk for developing related complications.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Frequent dehydration
- Low blood pressure
- Muscle weakness or cramps
- Excessive urination
- Family history of Bartter syndrome
should consider undergoing this genetic test. Additionally, those with risk factors related to kidney disorders may benefit from testing.
Benefits of Taking the Test
- Early detection of genetic predisposition to Bartter syndrome.
- Informed decision-making regarding health management.
- Guidance for family planning and genetic counseling.
- Personalized treatment options based on genetic findings.
Understanding Your Results
Results from the SLC12A2 Gene Bartter Syndrome NGS Genetic DNA Test can provide insight into your genetic risks. A genetic counselor will help interpret these results, discussing their implications for your health and any necessary follow-up actions.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
Don’t wait to take control of your health! Book the SLC12A2 Gene Bartter Syndrome NGS Genetic DNA Test today. For inquiries or to schedule your test, please call or WhatsApp us at +2348077798758.
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 and a genetic counseling session to draw a pedigree chart of family members affected with the SLC12A2 gene.
This test is essential for individuals at risk and is conducted under the specialty of General Physicians within the Genetics department. It addresses diseases related to Hepatology, Nephrology, and Endocrinology Disorders.
