TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test
At DNA Labs UAE, we offer the TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test for individuals experiencing symptoms related to this condition. This comprehensive test provides valuable insights into the underlying genetic cause of Adrenocorticotropic Hormone (ACTH) deficiency.
Test Components
The TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test includes:
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Hepatology, Nephrology, Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Test Price
The cost of the TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test is AED 4400.0.
Pre-Test Information
Prior to undergoing the TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the TBX19 gene.
Test Details
The TBX19 gene is responsible for producing a protein called T-box transcription factor 19. This protein plays a crucial role in the development and function of the pituitary gland, located at the base of the brain.
Adrenocorticotropic hormone (ACTH) deficiency is characterized by a lack of production of ACTH, which stimulates the adrenal glands to produce cortisol. Cortisol is essential for regulating various bodily functions, including metabolism, immune response, and stress response.
NGS (Next-Generation Sequencing) genetic testing is a cutting-edge technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. This type of testing can identify genetic mutations or variations associated with specific conditions, such as ACTH deficiency.
The TBX19 Gene Adrenocorticotropic Hormone Deficiency NGS Genetic Test involves sequencing the TBX19 gene using NGS technology to identify any mutations or variations that may be linked to ACTH deficiency. This test helps in diagnosing the underlying genetic cause of ACTH deficiency and guides appropriate treatment and management options.
For more information or to schedule an appointment for the TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test, please contact DNA Labs UAE.
Test Name | TBX19 Gene Adrenocorticotropic hormone deficiency Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Hepatology Nephrology Endocrinology Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for TBX19 Gene Adrenocorticotropic hormone deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX19 Gene Adrenocorticotropic hormone deficiency NGS Genetic DNA Test gene TBX19 |
Test Details | The TBX19 gene is responsible for producing a protein called T-box transcription factor 19. This protein plays a crucial role in the development and function of the pituitary gland, which is a small gland located at the base of the brain. Adrenocorticotropic hormone (ACTH) deficiency is a condition characterized by a lack of production of ACTH, which is a hormone that stimulates the adrenal glands to produce cortisol. Cortisol is an important hormone that helps regulate various bodily functions, including metabolism, immune response, and stress response. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. It can be used to identify genetic mutations or variations that may be responsible for a particular condition, such as ACTH deficiency. Therefore, a TBX19 gene adrenocorticotropic hormone deficiency NGS genetic test would involve sequencing the TBX19 gene using next-generation sequencing technology to identify any mutations or variations that may be associated with ACTH deficiency. This test can help in diagnosing the underlying genetic cause of ACTH deficiency and guide appropriate treatment and management options. |