TNFRSF11B Gene Paget disease juvenile Genetic Test
At DNA Labs UAE, we offer the TNFRSF11B Gene Paget disease juvenile Genetic Test at a cost of AED 4400.0.
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: Osteology Dermatology Immunology Disorders
Doctor and Test Department
This test is performed by a Dermatologist in our Genetics department.
Pre Test Information
Prior to undergoing the TNFRSF11B Gene Paget disease juvenile Genetic Test, it is important 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 with TNFRSF11B Gene Paget disease, juvenile NGS Genetic DNA Test gene TNFRSF11B.
Test Details
The TNFRSF11B gene is associated with Paget disease, juvenile, a rare genetic disorder characterized by abnormal bone remodeling. Mutations in this gene can lead to overactive osteoclasts, which are responsible for breaking down and remodeling bone tissue. Symptoms of Paget disease, juvenile include enlarged and misshapen bones, bone pain, fractures, and other complications.
Our NGS (Next-Generation Sequencing) genetic testing method allows for the analysis of multiple genes simultaneously for variations or mutations. In the context of Paget disease, juvenile, NGS genetic testing can identify specific mutations in the TNFRSF11B gene that may be responsible for the condition. This testing can help confirm a diagnosis, guide treatment decisions, and provide information about the likelihood of passing the condition on to future generations.
It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness, benefits, and limitations of NGS genetic testing for Paget disease, juvenile, and to understand the potential implications of the test results.
| Test Name | TNFRSF11B Gene Paget disease juvenile 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TNFRSF11B Gene Paget disease, juvenile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNFRSF11B Gene Paget disease, juvenile NGS Genetic DNA Test gene TNFRSF11B |
| Test Details |
The TNFRSF11B gene is associated with Paget disease, juvenile, which is a rare genetic disorder characterized by abnormal bone remodeling. Mutations in this gene can lead to overactive osteoclasts, which are cells responsible for breaking down and remodeling bone tissue. This excessive bone remodeling can result in enlarged and misshapen bones, bone pain, fractures, and other complications. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for variations or mutations. In the context of Paget disease, juvenile, NGS genetic testing can identify specific mutations in the TNFRSF11B gene that may be responsible for the condition. This testing can help confirm a diagnosis, guide treatment decisions, and provide information about the likelihood of passing the condition on to future generations. It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness, benefits, and limitations of NGS genetic testing for Paget disease, juvenile, and to understand the potential implications of the test results. |
