HSD11B2 Gene Apparent Mineralocorticoid Excess NGS Genetic DNA Test
Introduction
The HSD11B2 Gene Apparent Mineralocorticoid Excess NGS Genetic DNA Test is a specialized genetic assessment that plays a critical role in diagnosing conditions associated with metabolic disorders. This test utilizes Next Generation Sequencing (NGS) technology to analyze genetic variations that may lead to apparent mineralocorticoid excess, a condition that can significantly affect blood pressure and electrolyte balance.
What the Test Measures
This test specifically measures mutations in the HSD11B2 gene, which encodes an enzyme responsible for converting active cortisol into inactive cortisone. Abnormalities in this gene can result in excess cortisol activity, leading to various health complications.
Who Should Consider This Test
Individuals experiencing symptoms such as hypertension, hypokalemia (low potassium levels), or metabolic disorders should consider the HSD11B2 Gene Test. Additionally, those with a family history of apparent mineralocorticoid excess or related metabolic disorders are encouraged to undergo this testing for early diagnosis and management.
Benefits of Taking the Test
- Early identification of genetic predispositions to mineralocorticoid excess.
- Informed decision-making regarding treatment options.
- Guidance for lifestyle changes to manage symptoms effectively.
- Enhanced understanding of family health history.
Understanding Your Results
Results from the HSD11B2 Gene Test will provide insights into the presence of genetic mutations. A genetic counseling session is recommended to help interpret the results and discuss potential implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| HSD11B2 Gene Apparent Mineralocorticoid Excess NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To take the next step in understanding your health, book the HSD11B2 Gene Apparent Mineralocorticoid Excess NGS Genetic DNA Test today. For more information or to schedule your appointment, 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: Clinical History of Patient who is going for HSD11B2 Gene Test; Genetic Counseling session to draw a pedigree chart of affected family members.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
