TCTN1 Gene Joubert syndrome type 13 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 TCTN1 Gene Joubert syndrome type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN1 Gene Joubert syndrome type 13.
Test Details:
The TCTN1 gene is associated with Joubert syndrome type 13, a rare genetic disorder that affects the development of the brain. Joubert syndrome is characterized by abnormal breathing patterns, impaired coordination, intellectual disability, and other neurological abnormalities.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous sequencing of multiple genes, including the TCTN1 gene, to identify any variations or mutations that may be present. This type of testing can help diagnose Joubert syndrome type 13 and provide information about the specific genetic cause of the disorder.
If you suspect that you or someone you know may have Joubert syndrome type 13, a healthcare professional can order a NGS genetic test to confirm the diagnosis. The test involves collecting a sample of blood or saliva, which is then sent to a laboratory for analysis. The results of the test can help guide treatment and management strategies for individuals with Joubert syndrome type 13.
Test Name | TCTN1 Gene Joubert syndrome type 13 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 TCTN1 Gene Joubert syndrome type 13 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TCTN1 Gene Joubert syndrome type 13 |
Test Details |
The TCTN1 gene is associated with Joubert syndrome type 13, a rare genetic disorder that affects the development of the brain. Joubert syndrome is characterized by abnormal breathing patterns, impaired coordination, intellectual disability, and other neurological abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It allows for the simultaneous sequencing of multiple genes, including the TCTN1 gene, to identify any variations or mutations that may be present. This type of testing can help diagnose Joubert syndrome type 13 and provide information about the specific genetic cause of the disorder. If you suspect that you or someone you know may have Joubert syndrome type 13, a healthcare professional can order a NGS genetic test to confirm the diagnosis. The test involves collecting a sample of blood or saliva, which is then sent to a laboratory for analysis. The results of the test can help guide treatment and management strategies for individuals with Joubert syndrome type 13. |