WRN Gene Werner Syndrome Genetic Test
Test Name: WRN Gene Werner syndrome Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 WRN Gene Werner syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WRN Gene Werner syndrome NGS Genetic DNA Test gene WRN
Test Details
WRN gene Werner syndrome NGS genetic test is a type of genetic test that specifically looks for mutations or variations in the WRN gene associated with Werner syndrome. Werner syndrome is a rare genetic disorder characterized by premature aging, short stature, and an increased risk of developing age-related diseases such as cancer, heart disease, and diabetes.
NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of the WRN gene, NGS can be used to identify any mutations or variations that may be present in the gene, which can help in diagnosing Werner syndrome.
The WRN gene provides instructions for producing a protein called WRN, which is involved in maintaining the stability and integrity of DNA. Mutations in this gene can impair the function of the WRN protein, leading to the characteristic features of Werner syndrome.
The WRN gene Werner syndrome NGS genetic test involves obtaining a DNA sample, typically through a blood or saliva sample, and analyzing it using NGS technology. The DNA is sequenced, and any variations or mutations in the WRN gene are identified and analyzed to determine if they are disease-causing.
This genetic test can be useful in diagnosing Werner syndrome in individuals with symptoms suggestive of the disorder, as well as in identifying carriers of the WRN gene mutation who may be at risk of passing it on to their children. It can also help in genetic counseling and family planning decisions.
It is important to note that genetic testing for Werner syndrome should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. They can provide guidance and support in understanding the test results and their implications.
| Test Name | WRN Gene Werner 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 WRN Gene Werner syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WRN Gene Werner syndrome NGS Genetic DNA Test gene WRN |
| Test Details | WRN gene Werner syndrome NGS genetic test is a type of genetic test that specifically looks for mutations or variations in the WRN gene associated with Werner syndrome. Werner syndrome is a rare genetic disorder characterized by premature aging, short stature, and an increased risk of developing age-related diseases such as cancer, heart disease, and diabetes. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of the WRN gene, NGS can be used to identify any mutations or variations that may be present in the gene, which can help in diagnosing Werner syndrome. The WRN gene provides instructions for producing a protein called WRN, which is involved in maintaining the stability and integrity of DNA. Mutations in this gene can impair the function of the WRN protein, leading to the characteristic features of Werner syndrome. The WRN gene Werner syndrome NGS genetic test involves obtaining a DNA sample, typically through a blood or saliva sample, and analyzing it using NGS technology. The DNA is sequenced, and any variations or mutations in the WRN gene are identified and analyzed to determine if they are disease-causing. This genetic test can be useful in diagnosing Werner syndrome in individuals with symptoms suggestive of the disorder, as well as in identifying carriers of the WRN gene mutation who may be at risk of passing it on to their children. It can also help in genetic counseling and family planning decisions. It is important to note that genetic testing for Werner syndrome should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. They can provide guidance and support in understanding the test results and their implications. |
