ELN Gene Supravalvar Aortic Stenosis Genetic Test
Welcome to DNA Labs UAE, where we offer the ELN Gene Supravalvar Aortic Stenosis Genetic Test. This test is designed to identify variations or mutations in the ELN gene associated with supravalvar aortic stenosis (SVAS).
Test Details
Supravalvar aortic stenosis is a heart condition characterized by a narrowing of the aorta just above the valve, resulting in restricted blood flow from the heart. This condition is often caused by mutations in the ELN gene, which is responsible for producing elastin, an important component of connective tissues in the body, including blood vessels.
Our ELN Gene Supravalvar Aortic Stenosis Genetic Test utilizes NGS (Next-Generation Sequencing) technology. NGS is a high-throughput DNA sequencing method that allows for the rapid and accurate analysis of large amounts of genetic material. With NGS, we can simultaneously analyze multiple genes, including the ELN gene, to identify any variations or mutations that may be present.
Test Components and Price
The ELN Gene Supravalvar Aortic Stenosis Genetic Test is priced at 4400.0 AED. The test can be performed using a blood sample, extracted DNA, or even a single drop of blood on an FTA Card.
Report Delivery and Test Type
After the sample is collected, the report will be delivered within 3 to 4 weeks. The ELN Gene Supravalvar Aortic Stenosis Genetic Test falls under the category of Vascular Diseases.
Referring Doctor and Test Department
For this test, you can consult a General Physician. The test will be conducted in our Genetics department.
Pre Test Information
Prior to undergoing the ELN Gene Supravalvar Aortic Stenosis Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by ELN Gene Supravalvar Aortic Stenosis NGS Genetic DNA Test gene ELN.
Importance of the Test
By performing the ELN Gene Supravalvar Aortic Stenosis Genetic Test, healthcare professionals can determine if there are any genetic variations or mutations in the ELN gene that may be contributing to the development of SVAS. This information is crucial for diagnosing the condition, understanding its inheritance pattern, and providing appropriate medical management and genetic counseling to affected individuals and their families.
| Test Name | ELN Gene Supravalvar aortic stenosis 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 ELN Gene Supravalvar aortic stenosis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ELN Gene Supravalvar aortic stenosis NGS Genetic DNA Test gene ELN |
| Test Details | ELN gene supravalvar aortic stenosis NGS genetic test is a type of genetic test that looks for variations or mutations in the ELN gene associated with supravalvar aortic stenosis (SVAS). Supravalvar aortic stenosis is a heart condition where there is a narrowing of the aorta just above the valve, leading to restricted blood flow from the heart. This condition is often caused by mutations in the ELN gene, which provides instructions for making a protein called elastin. Elastin is an important component of the connective tissues in the body, including the blood vessels. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid and accurate sequencing of large amounts of genetic material. In the context of genetic testing, NGS can be used to analyze multiple genes simultaneously, including the ELN gene, to identify any variations or mutations that may be present. By performing an ELN gene supravalvar aortic stenosis NGS genetic test, healthcare professionals can determine if there are any genetic variations or mutations in the ELN gene that may be contributing to the development of SVAS. This information can help in diagnosing the condition, understanding its inheritance pattern, and providing appropriate medical management and genetic counseling to affected individuals and their families. |
