SOX17 Gene Vesicoureteral reflux type 3 Genetic Test
Welcome to DNA Labs UAE, where we offer the SOX17 Gene Vesicoureteral reflux type 3 Genetic Test. This test can help diagnose and identify individuals at risk of developing type 3 vesicoureteral reflux (VUR). Read on to learn more about the test, its cost, symptoms, diagnosis, and other important details.
Test Details
The SOX17 gene is associated with vesicoureteral reflux (VUR), specifically type 3 VUR. VUR is a condition where urine flows backward from the bladder into the ureters and sometimes up into the kidneys. This can lead to urinary tract infections, kidney damage, and other complications.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations that may be associated with a particular condition or disease. A genetic test for SOX17 gene mutations using NGS can help identify individuals who are at risk of developing type 3 VUR. It can also aid in genetic counseling and family planning for individuals with a family history of VUR.
Test Components and Price
- Test Name: SOX17 Gene Vesicoureteral reflux type 3 Genetic Test
- Components: Blood or Extracted DNA or One drop Blood on FTA Card
- Price: 4400.0 AED
Report Delivery
The report for the SOX17 Gene Vesicoureteral reflux type 3 Genetic Test will be delivered within 3 to 4 weeks.
Method
The SOX17 Gene Vesicoureteral reflux type 3 Genetic Test is performed using NGS (Next-Generation Sequencing) technology.
Test Type
The test falls under the following medical specialties: Hepatology, Nephrology, and Endocrinology Disorders.
Doctor and Test Department
The test can be ordered by a General Physician and is conducted in the Genetics department.
Pre Test Information
Prior to undergoing the SOX17 Gene Vesicoureteral reflux type 3 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 the SOX17 Gene Vesicoureteral reflux type 3 NGS Genetic DNA Test gene SOX17.
Diagnosis and Genetic Testing
It’s important to note that genetic testing for VUR is not typically performed as a standalone diagnostic tool. The diagnosis of VUR is usually made based on clinical symptoms, imaging studies, and other tests. However, genetic testing is often recommended for individuals with a family history of VUR or in cases where the cause of VUR is unclear.
If you suspect you or someone you know may have VUR or a genetic predisposition to VUR, it’s best to consult with a healthcare professional or a genetic counselor who can provide further guidance and information about the available genetic testing options.
Test Name | SOX17 Gene Vesicoureteral reflux type 3 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 | Hepatology Nephrology Endocrinology Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for SOX17 Gene Vesicoureteral reflux type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOX17 Gene Vesicoureteral reflux type 3 NGS Genetic DNA Test gene SOX17 |
Test Details |
The SOX17 gene is associated with vesicoureteral reflux (VUR), specifically type 3 VUR. VUR is a condition where urine flows backward from the bladder into the ureters and sometimes up into the kidneys. This can lead to urinary tract infections, kidney damage, and other complications. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations that may be associated with a particular condition or disease. A genetic test for SOX17 gene mutations using NGS can help identify individuals who are at risk of developing type 3 VUR. It can also aid in genetic counseling and family planning for individuals with a family history of VUR. It’s important to note that genetic testing for VUR is not typically performed as a standalone diagnostic tool. The diagnosis of VUR is usually made based on clinical symptoms, imaging studies, and other tests. Genetic testing is often recommended for individuals with a family history of VUR or in certain cases where the cause of VUR is unclear. If you suspect you or someone you know may have VUR or a genetic predisposition to VUR, it’s best to consult with a healthcare professional or a genetic counselor who can provide further guidance and information about the available genetic testing options. |