TCTN3 Gene Joubert Syndrome Type 18 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for TCTN3 Gene Joubert syndrome type 18 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN3 Gene Joubert syndrome type 18.
Test Details
The TCTN3 gene is associated with Joubert syndrome type 18, which is a rare genetic disorder characterized by developmental delay, intellectual disability, breathing abnormalities, and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Joubert syndrome type 18, NGS genetic testing can be used to analyze the TCTN3 gene for any mutations or variations that may be causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in the genes of interest. This can help in confirming a diagnosis, understanding the genetic basis of the disorder, and providing information for genetic counseling and family planning. It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 18 and to understand the potential implications of the test results.
Test Name | TCTN3 Gene Joubert syndrome type 18 Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for TCTN3 Gene Joubert syndrome type 18 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN3 Gene Joubert syndrome type 18 |
Test Details |
The TCTN3 gene is associated with Joubert syndrome type 18, which is a rare genetic disorder characterized by developmental delay, intellectual disability, breathing abnormalities, and distinctive facial features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Joubert syndrome type 18, NGS genetic testing can be used to analyze the TCTN3 gene for any mutations or variations that may be causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in the genes of interest. This can help in confirming a diagnosis, understanding the genetic basis of the disorder, and providing information for genetic counseling and family planning. It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Joubert syndrome type 18 and to understand the potential implications of the test results. |