TBX19 Gene Adrenocorticotropic Hormone Deficiency NGS Genetic DNA Test
Introduction
The TBX19 Gene Adrenocorticotropic Hormone Deficiency NGS Genetic DNA Test is a specialized genetic examination aimed at identifying mutations in the TBX19 gene, which are responsible for adrenocorticotropic hormone deficiency. This condition can lead to significant hormonal imbalances and associated health issues. Understanding your genetic predisposition is vital for effective management and treatment of related disorders.
What the Test Measures
This test detects mutations in the TBX19 gene, which plays a crucial role in the production of adrenocorticotropic hormone (ACTH). ACTH is essential for regulating cortisol levels in the body, and deficiencies can lead to serious health complications.
Who Should Consider This Test
Individuals experiencing symptoms such as fatigue, weight loss, low blood pressure, or other signs of adrenal insufficiency should consider this test. Those with a family history of hormonal disorders or genetic predispositions may also benefit from this examination.
Benefits of Taking the Test
- Accurate identification of genetic mutations affecting hormone production.
- Informed decision-making regarding treatment options and lifestyle changes.
- Early detection of potential health issues related to hormonal imbalances.
- Access to tailored genetic counseling for affected individuals and families.
Understanding Your Results
Results from the TBX19 Gene Adrenocorticotropic Hormone Deficiency NGS Genetic DNA Test will provide insights into the presence of genetic mutations. A genetic counselor will help you interpret these results and discuss potential implications for your health and that of your family.
Test Pricing
Discount Price | Regular Price |
---|---|
400,000 NGN | 560,000 NGN |
Booking the Test
To book the TBX19 Gene Adrenocorticotropic Hormone Deficiency NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you with scheduling and any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by TBX19 gene defects.
For more information, feel free to reach out or visit our website. Your health is our priority!