KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test
Introduction to the Test
The KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test is a pivotal diagnostic tool designed to identify mutations in the KLHL3 gene, which are associated with pseudohypoaldosteronism type 2, a rare genetic disorder that affects the body’s ability to regulate sodium and potassium levels. This test is vital for individuals with a family history of this condition or those exhibiting symptoms related to vascular diseases.
What the Test Measures
This genetic test detects specific mutations within the KLHL3 gene using Next Generation Sequencing (NGS) technology. By analyzing the genetic material, the test provides insights into the likelihood of developing pseudohypoaldosteronism type 2, enabling proactive management of health.
Who Should Consider This Test?
Individuals who should consider the KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test include:
- Those with a family history of pseudohypoaldosteronism or related vascular diseases.
- Patients exhibiting symptoms such as hypertension, hyperkalemia, or metabolic acidosis.
- Individuals seeking genetic counseling to understand their risk factors regarding this condition.
Benefits of Taking the Test
- Early detection of genetic predispositions, allowing for timely intervention.
- Informed decision-making for family planning and management of health risks.
- Access to personalized healthcare strategies based on genetic insights.
Understanding Your Results
Results from the KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test will provide information on whether mutations are present in the KLHL3 gene. A genetic counselor will help interpret the results, guiding you through the implications and potential next steps in your healthcare journey.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the KLHL3 Gene Pseudohypoaldosteronism Type 2D NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to schedule your appointment. Ensure you have a clinical history ready and consider a genetic counseling session to discuss your family’s medical history.
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required can be blood, extracted DNA, or one drop of blood on an FTA card.
Pre-Test Instructions
Prior to the test, it is essential to have a detailed clinical history of the patient and participate in a genetic counseling session to create a pedigree chart of family members affected by the KLHL3 gene.
