DBH Gene Dopamine Beta-Hydroxylase Deficiency NGS Genetic DNA Test
Introduction to the Test
The DBH Gene Dopamine Beta-Hydroxylase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that plays a crucial role in identifying genetic disorders related to cardiovascular and pneumology issues. This test leverages Next-Generation Sequencing (NGS) technology to analyze the DBH gene, which is responsible for encoding the enzyme dopamine beta-hydroxylase, essential for converting dopamine to norepinephrine.
What the Test Measures
This genetic test measures the presence of mutations in the DBH gene that may lead to dopamine beta-hydroxylase deficiency. By identifying these mutations, healthcare providers can better understand the underlying causes of cardiovascular and pneumology disorders in patients.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Severe hypotension
- Syncope (fainting)
- Cardiovascular complications
Moreover, those with a family history of cardiovascular or pneumology disorders are encouraged to consider this test to assess their genetic risk factors.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions related to dopamine beta-hydroxylase deficiency.
- Informed decision-making regarding treatment options.
- Understanding of familial risk for inherited conditions.
- Access to tailored management plans based on genetic findings.
Understanding Your Results
Once the test is completed, results will indicate whether mutations are present in the DBH gene. A genetic counselor will assist in interpreting the results and discussing potential implications for treatment and lifestyle adjustments.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DBH Gene Dopamine Beta-Hydroxylase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book your DBH Gene Dopamine Beta-Hydroxylase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team is ready to assist you in taking this important step towards better health.
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 affected family members.
