SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test
Introduction
The SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test is an advanced diagnostic test that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the SLC12A7 gene associated with Bartter syndrome. This condition is characterized by a group of renal tubular disorders that affect electrolyte balance, leading to various health complications. Understanding the genetic basis of this syndrome is crucial for effective management and treatment.
What the Test Measures
This test specifically measures genetic variations in the SLC12A7 gene, which plays a significant role in kidney function and electrolyte regulation. Detecting mutations in this gene can provide insights into the underlying causes of Bartter syndrome.
Who Should Consider This Test
Individuals who may benefit from the SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test include:
- Patients with symptoms such as excessive thirst, frequent urination, and dehydration.
- Individuals with a family history of Bartter syndrome or related kidney disorders.
- Those experiencing unexplained electrolyte imbalances.
Benefits of Taking the Test
Taking the SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test offers several benefits:
- Accurate Diagnosis: Identifies specific genetic mutations, leading to a precise diagnosis.
- Informed Treatment Decisions: Helps healthcare providers tailor treatment plans based on genetic findings.
- Family Planning: Provides valuable information for affected families regarding the inheritance of the condition.
Understanding Your Results
Results from the SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test will be reviewed by a qualified genetic counselor or physician. They will explain the implications of the findings, discuss potential treatment options, and provide guidance on managing the condition.
Test Name and Price
Test Name | Discount Price | Regular Price |
---|---|---|
SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history and a genetic counseling session to draw a pedigree chart of family members affected with Bartter syndrome is recommended.
Book Your Test Today!
We have branches across all major cities in Kenya, offering convenient access to this important genetic test. To book the SLC12A7 Gene Bartter Syndrome NGS Genetic DNA Test or for more information, please call or WhatsApp us at +254713408028.