ACTG1 Gene Baraitser-Winter syndrome type 2 Genetic Test
Components
- Price: 4400.0 AED
- Sample Condition: Blood
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for ACTG1 Gene Baraitser-Winter syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTG1 Gene Baraitser-Winter syndrome type 2 NGS Genetic DNA Test gene ACTG1.
Test Details
The ACTG1 gene is associated with a rare genetic disorder called Baraitser-Winter syndrome type 2. This syndrome is characterized by intellectual disability, facial dysmorphism, and various physical abnormalities.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any mutations or variations that may be present. In the case of Baraitser-Winter syndrome type 2, NGS testing can be used to analyze the ACTG1 gene to determine if there are any mutations or variations that may be causing the syndrome.
This type of genetic testing can help in confirming a diagnosis, providing information about the prognosis, and guiding treatment decisions. It can also be useful for genetic counseling and family planning purposes.
It is important to consult with a genetic counselor or a healthcare professional who specializes in genetics to discuss the benefits, limitations, and potential risks of genetic testing before undergoing the test. They can provide further information and guidance based on your specific situation.
Test Name | ACTG1 Gene Baraitser-Winter syndrome type 2 Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for ACTG1 Gene Baraitser-Winter syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTG1 Gene Baraitser-Winter syndrome type 2 NGS Genetic DNA Test gene ACTG1 |
Test Details |
The ACTG1 gene is associated with a rare genetic disorder called Baraitser-Winter syndrome type 2. This syndrome is characterized by intellectual disability, facial dysmorphism, and various physical abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any mutations or variations that may be present. In the case of Baraitser-Winter syndrome type 2, NGS testing can be used to analyze the ACTG1 gene to determine if there are any mutations or variations that may be causing the syndrome. This type of genetic testing can help in confirming a diagnosis, providing information about the prognosis, and guiding treatment decisions. It can also be useful for genetic counseling and family planning purposes. It is important to consult with a genetic counselor or a healthcare professional who specializes in genetics to discuss the benefits, limitations, and potential risks of genetic testing before undergoing the test. They can provide further information and guidance based on your specific situation. |