chr. 7q11.23 Gene Williams-Beuren syndrome Genetic Test
At DNA Labs UAE, we offer the chr. 7q11.23 Gene Williams-Beuren syndrome Genetic Test for individuals who suspect they may have Williams-Beuren syndrome (WBS). This test is designed to analyze the genes in the 7q11.23 region of chromosome 7, which is associated with WBS.
Test Details
The chr. 7q11.23 gene refers to a specific region on chromosome 7, known as 7q11.23. This region contains several genes, one of which is associated with Williams-Beuren syndrome (WBS). Williams-Beuren syndrome is a rare genetic disorder characterized by various physical and developmental features. It is caused by a deletion of genetic material on chromosome 7, specifically in the 7q11.23 region. This deletion affects the expression of several genes, including the elastin gene, which is responsible for the connective tissue in the body.
Our chr. 7q11.23 Gene Williams-Beuren syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This advanced sequencing technology allows us to identify the specific genetic mutation or deletion in the 7q11.23 region that is responsible for the syndrome.
Test Components and Price
Test Name: chr. 7q11.23 Gene Williams-Beuren syndrome Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Before undergoing the chr. 7q11.23 Gene Williams-Beuren syndrome 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 with chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic DNA Test gene chr. 7q11.23.
Benefits of the Test
NGS genetic testing for Williams-Beuren syndrome can help in various ways:
- Confirm a diagnosis
- Provide information about the severity of the condition
- Guide medical management and treatment options
- Carrier testing in families with a history of the syndrome
- Prenatal testing for families with a history of the syndrome
Overall, the chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic Test is a specific genetic test that uses NGS technology to analyze the genes in the 7q11.23 region for the presence of mutations or deletions associated with Williams-Beuren syndrome.
| Test Name | chr. 7q11.23 Gene Williams-Beuren syndrome 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic DNA Test gene chr. 7q11.23 |
| Test Details |
The chr. 7q11.23 gene refers to a specific region on chromosome 7, known as 7q11.23. This region contains several genes, one of which is associated with Williams-Beuren syndrome (WBS). Williams-Beuren syndrome is a rare genetic disorder characterized by various physical and developmental features. It is caused by a deletion of genetic material on chromosome 7, specifically in the 7q11.23 region. This deletion affects the expression of several genes, including the elastin gene, which is responsible for the connective tissue in the body. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Williams-Beuren syndrome, NGS genetic testing can be used to identify the specific genetic mutation or deletion in the 7q11.23 region that is responsible for the syndrome. NGS genetic testing for Williams-Beuren syndrome can help confirm a diagnosis, provide information about the severity of the condition, and guide medical management and treatment options. It can also be used for carrier testing and prenatal testing in families with a history of the syndrome. Overall, the chr. 7q11.23 Gene Williams-Beuren syndrome NGS Genetic Test is a specific genetic test that uses NGS technology to analyze the genes in the 7q11.23 region for the presence of mutations or deletions associated with Williams-Beuren syndrome. |
