CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test
Are you concerned about your reproductive health? The CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test offered by DNA Labs UAE can provide you with valuable insights. This blog will provide detailed information about the test, its components, cost, symptoms, diagnosis, and more.
Test Details
The CFTR gene, also known as the cystic fibrosis transmembrane conductance regulator gene, plays a crucial role in regulating salt and fluid flow in organs like the lungs, pancreas, and reproductive system. Congenital bilateral absence of vas deferens (CBAVD) is a condition where the vas deferens, the tubes responsible for carrying sperm from the testicles to the urethra, are either missing or blocked. This condition can lead to male infertility.
Our CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. By focusing on the CFTR gene, healthcare professionals can identify specific mutations or variations that may be associated with CBAVD. This information can aid in diagnosing the condition, determining the risk of passing it on to future generations, and guiding treatment options such as assisted reproductive techniques.
It is important to note that while CFTR gene mutations are a common cause of CBAVD, other genetic and non-genetic factors can also contribute to its development. Therefore, our genetic testing for CBAVD may involve analyzing other genes or factors in addition to the CFTR gene.
Test Components and Price
The CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test is available at a cost of AED 4400.0. The test can be performed using either blood or extracted DNA, or even a single drop of blood on an FTA card.
Report Delivery and Method
After undergoing the CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test, you can expect to receive your report within 3 to 4 weeks. Our advanced NGS technology ensures accurate and efficient analysis of the CFTR gene.
Referring Doctor and Test Department
Our CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test is conducted under the supervision of experienced gynecologists. The test falls under the genetics department, where our experts specialize in reproductive disorders.
Pre-Test Information
Before undergoing the CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test, it is recommended 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 by CBAVD and the CFTR gene.
Conclusion
If you suspect or have been diagnosed with Congenital Bilateral Absence of Vas Deferens, our CFTR Gene Congenital Bilateral Absence of Vas Deferens Genetic Test can provide valuable insights into your condition. By analyzing the CFTR gene using NGS technology, we can identify specific mutations or variations that may be causing CBAVD. This information can aid in diagnosis, risk assessment, and treatment planning. Contact DNA Labs UAE today to schedule your test and take control of your reproductive health.
| Test Name | CFTR Gene Congenital bilateral absence of vas deferens 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 | Reproductive Disorders |
| Doctor | Gynecology |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for CFTR Gene Congenital bilateral absence of vas deferens NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFTR Gene Congenital bilateral absence of vas deferens NGS Genetic DNA Test gene CFTR |
| Test Details | The CFTR gene (cystic fibrosis transmembrane conductance regulator gene) is responsible for producing a protein that regulates the flow of salt and fluids in various organs, including the lungs, pancreas, and reproductive system. Congenital bilateral absence of vas deferens (CBAVD) is a condition where the vas deferens, the tubes that carry sperm from the testicles to the urethra, are missing or blocked. This condition can lead to infertility in males. 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 CBAVD, NGS genetic testing can be used to identify mutations or variations in the CFTR gene that may be associated with the condition. By analyzing the CFTR gene using NGS technology, healthcare professionals can identify specific mutations or variations that may be causing CBAVD. This information can be helpful in diagnosing the condition, determining the risk of passing it on to future generations, and guiding treatment options such as assisted reproductive techniques. It is important to note that while CFTR gene mutations are a common cause of CBAVD, not all individuals with CBAVD will have CFTR gene mutations. Other genetic and non-genetic factors can also contribute to the development of CBAVD. Therefore, genetic testing for CBAVD may involve analyzing other genes or factors in addition to the CFTR gene. |
