AGTR2 Gene Mental retardation X-linked type 88 AGTR2 related Genetic Test
Are you concerned about mental retardation in your family? DNA Labs UAE offers the AGTR2 Gene Mental retardation X-linked type 88 AGTR2 related Genetic Test to help diagnose and understand this condition. With a price of 4400.0 AED, this test is an important tool in identifying and managing genetic disorders.
Test Details
The AGTR2 gene plays a crucial role in regulating blood pressure and the development of various organs and tissues in the body. Mutations or changes in this gene can lead to mental retardation, specifically X-linked type 88 (MRX88). This rare genetic disorder primarily affects males and is characterized by intellectual disability, delayed speech and language development, and behavioral problems.
Our AGTR2-related NGS genetic testing utilizes advanced sequencing technology to analyze multiple genes simultaneously. By focusing on the AGTR2 gene, we aim to identify any mutations or changes that may be associated with MRX88 or other related conditions. This information can be invaluable for genetic counseling, family planning, and guiding treatment options or management strategies.
Pre Test Information
Prior to undergoing the AGTR2 Gene Mental retardation X-linked type 88 AGTR2 related Genetic Test, it is important to provide a clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by AGTR2 Gene Mental retardation, X-linked type 88, AGTR2 related.
Test Components
- Price: 4400.0 AED
- Sample Condition: Blood
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test type: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
It is essential to consult with a healthcare professional or genetic counselor to fully understand the implications of AGTR2-related NGS genetic testing in the context of an individual’s medical history and family situation. This test can provide valuable information for making informed decisions about genetic conditions, family planning, and potential treatment options.
Test Name | AGTR2 Gene Mental retardation X-linked type 88 AGTR2 related Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for AGTR2 Gene Mental retardation, X-linked type 88, AGTR2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with AGTR2 Gene Mental retardation, X-linked type 88, AGTR2 related |
Test Details |
The AGTR2 gene is responsible for providing instructions for making a protein called angiotensin II receptor type 2. This protein is involved in regulating blood pressure and the development of various organs and tissues in the body. Mutations or changes in the AGTR2 gene can lead to a condition known as mental retardation, X-linked type 88 (MRX88). This is a rare genetic disorder that primarily affects males. Individuals with MRX88 typically have intellectual disability, delayed speech and language development, and may exhibit behavioral problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of AGTR2-related NGS genetic testing, it aims to identify mutations or changes in the AGTR2 gene that may be associated with MRX88 or other related conditions. AGTR2-related NGS genetic testing can help in the diagnosis of MRX88 and provide information about the specific genetic changes in the AGTR2 gene. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options or management strategies. It’s important to consult with a healthcare professional or a genetic counselor to understand the specific details and implications of AGTR2-related NGS genetic testing in the context of an individual’s medical history and family situation. |