CUL3 Gene Pseudohypoaldosteronism Type 2E NGS Genetic DNA Test
Introduction
The CUL3 Gene Pseudohypoaldosteronism Type 2E NGS Genetic DNA Test is an advanced diagnostic tool that employs Next-Generation Sequencing (NGS) technology to analyze the CUL3 gene. This test is crucial for individuals who may be at risk for pseudohypoaldosteronism, a condition that affects the body’s ability to regulate sodium and potassium levels, leading to serious health complications.
What the Test Measures
This genetic test specifically measures mutations in the CUL3 gene, which are associated with pseudohypoaldosteronism type 2E. By identifying these mutations, healthcare providers can better understand a patient’s genetic predisposition to this condition.
Who Should Consider This Test
Individuals exhibiting symptoms such as hyperkalemia (high potassium levels), metabolic acidosis, or those with a family history of vascular diseases should consider this test. Additionally, patients with unexplained electrolyte imbalances may also benefit from genetic testing.
Benefits of Taking the Test
- Identifies genetic predispositions, enabling proactive health management.
- Guides treatment decisions based on genetic findings.
- Provides valuable information for family planning and genetic counseling.
- Enhances understanding of the condition, leading to better patient outcomes.
Understanding Your Results
Results from the CUL3 Gene Pseudohypoaldosteronism Type 2E NGS Genetic DNA Test will indicate whether mutations are present in the CUL3 gene. A genetic counselor will assist in interpreting the results, discussing implications for treatment, and providing guidance on next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today
To schedule your CUL3 Gene Pseudohypoaldosteronism Type 2E NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in understanding your genetic health and improving your well-being.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with CUL3 gene mutations.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Vascular Diseases
