SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test
Introduction
The SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test is a crucial diagnostic tool that helps identify genetic mutations associated with renal disorders. Understanding these genetic factors can significantly impact patient management and treatment strategies. This test employs Next-Generation Sequencing (NGS) technology to provide precise and comprehensive results, enabling healthcare providers to tailor interventions effectively.
What the Test Measures
This genetic test specifically measures variations in the SLC22A12 gene, which plays a vital role in uric acid transport in the kidneys. By detecting mutations in this gene, the test can determine an individual’s risk of developing hypouricemia and associated renal conditions.
Who Should Consider This Test?
Individuals who might benefit from this test include:
- Those with a family history of renal disorders or hypouricemia.
- Patients exhibiting symptoms such as recurrent kidney stones or unexplained renal dysfunction.
- Individuals with metabolic disorders that may be linked to uric acid levels.
Benefits of Taking the Test
The SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test offers several benefits:
- Accurate identification of genetic predispositions to renal disorders.
- Informed decision-making regarding lifestyle and treatment options.
- Enhanced understanding of family health risks through genetic counseling.
- Timely intervention that can prevent the progression of renal diseases.
Understanding Your Results
Results from the SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test are typically available within 3 to 4 weeks. A genetic counselor will provide guidance on interpreting the results, discussing potential implications for health management and family planning.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the SLC22A12 Gene Hypouricemia Renal Type 1 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your appointment and providing further information.
Pre-Test Instructions
Before taking the test, it is essential to have a clinical history assessment. A genetic counseling session is recommended to create a pedigree chart of family members affected by the SLC22A12 Gene Hypouricemia.
Specialty and Department
This test is conducted under the supervision of General Physicians in the Genetics department, focusing on Hepatology, Nephrology, and Endocrinology disorders.
