OFD1 Gene Joubert Syndrome Type 10 Genetic Test
Test Details
The OFD1 gene is associated with Joubert syndrome type 10. Joubert syndrome is a rare genetic disorder that affects the development of the brainstem and cerebellum, leading to various symptoms such as intellectual disability, breathing abnormalities, and characteristic facial features.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 10, NGS genetic testing can be used to identify mutations or variations in the OFD1 gene that may be responsible for the condition.
NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having Joubert syndrome type 10. It can help confirm the diagnosis, identify specific genetic variants, and provide information about the inheritance pattern of the condition.
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 10 in specific cases. They can provide guidance on the testing process, interpretation of results, and implications for individuals and their families.
Test Name
OFD1 Gene Joubert Syndrome Type 10 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 OFD1 Gene Joubert Syndrome Type 10 NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with OFD1 Gene Joubert Syndrome Type 10
| Test Name | OFD1 Gene Joubert syndrome type 10 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 OFD1 Gene Joubert syndrome type 10 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with OFD1 Gene Joubert syndrome type 10 |
| Test Details |
The OFD1 gene is associated with Joubert syndrome type 10. Joubert syndrome is a rare genetic disorder that affects the development of the brainstem and cerebellum, leading to various symptoms such as intellectual disability, breathing abnormalities, and characteristic facial features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Joubert syndrome type 10, NGS genetic testing can be used to identify mutations or variations in the OFD1 gene that may be responsible for the condition. NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having Joubert syndrome type 10. It can help confirm the diagnosis, identify specific genetic variants, and provide information about the inheritance pattern of the condition. 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 10 in specific cases. They can provide guidance on the testing process, interpretation of results, and implications for individuals and their families. |
