NR3C2 Gene Hypertension Early Onset Genetic Test
Welcome to DNA Labs UAE, where we offer the NR3C2 gene hypertension early onset genetic test. This test aims to identify any mutations or variations in the NR3C2 gene that may contribute to the development of early-onset hypertension.
Test Components and Price
- Components: Blood or Extracted DNA or One drop Blood on FTA Card
- Price: 4400.0 AED
Sample Condition
The sample required for this test can be either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
After the sample is collected, the report will be delivered within 3 to 4 weeks.
Method
This test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of genes, including the NR3C2 gene.
Test Type
The NR3C2 gene hypertension early onset genetic test falls under the category of vascular diseases.
Doctor
This test can be ordered by a general physician.
Test Department
The NR3C2 gene hypertension early onset genetic test is conducted in our Genetics department.
Pre Test Information
Before undergoing the NR3C2 gene hypertension early onset NGS genetic DNA test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the NR3C2 gene hypertension early onset NGS genetic DNA test gene NR3C2.
Test Details
The NR3C2 gene is responsible for encoding the mineralocorticoid receptor, which plays a crucial role in regulating blood pressure and fluid balance in the body. Mutations in the NR3C2 gene have been associated with early-onset hypertension, a condition characterized by high blood pressure that develops at a young age.
NGS genetic testing is a technique used to analyze the DNA sequence of genes, including the NR3C2 gene, in order to identify any mutations or variations that may be present. This type of genetic testing can provide valuable information about an individual’s genetic predisposition to early-onset hypertension and help guide treatment and management strategies.
By analyzing the NR3C2 gene through NGS genetic testing, healthcare professionals can identify specific mutations or variations that may be contributing to the development of early-onset hypertension. This information can be used to develop personalized treatment plans and interventions to effectively manage the condition.
It’s important to note that genetic testing alone may not be sufficient to diagnose or predict early-onset hypertension. It is typically used in conjunction with other clinical evaluations and assessments to provide a comprehensive understanding of an individual’s health and genetic profile. Additionally, genetic testing can also provide insights into an individual’s risk for other genetic conditions and diseases beyond hypertension.
Test Name | NR3C2 Gene Hypertension early onset 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 | Vascular Diseases |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for NR3C2 Gene Hypertension early onset NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NR3C2 Gene Hypertension early onset NGS Genetic DNA Test gene NR3C2 |
Test Details |
The NR3C2 gene is responsible for encoding the mineralocorticoid receptor, which plays a crucial role in regulating blood pressure and fluid balance in the body. Mutations in the NR3C2 gene have been associated with early-onset hypertension, a condition characterized by high blood pressure that develops at a young age. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of genes, including the NR3C2 gene, to identify any mutations or variations that may be present. This type of genetic testing can provide valuable information about an individual’s genetic predisposition to early-onset hypertension and help guide treatment and management strategies. By analyzing the NR3C2 gene through NGS genetic testing, healthcare professionals can identify specific mutations or variations that may be contributing to the development of early-onset hypertension. This information can be used to develop personalized treatment plans and interventions to manage the condition effectively. It’s important to note that genetic testing alone may not be sufficient to diagnose or predict early-onset hypertension. It is typically used in conjunction with other clinical evaluations and assessments to provide a comprehensive understanding of an individual’s health and genetic profile. Additionally, genetic testing can also provide insights into an individual’s risk for other genetic conditions and diseases beyond hypertension. |