CRPPA Gene Walker-Warburg syndrome Genetic Test
At DNA Labs UAE, we offer the CRPPA Gene Walker-Warburg syndrome 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Before undergoing the CRPPA Gene Walker-Warburg syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with CRPPA Gene Walker-Warburg syndrome.
Test Details
The CRPPA gene is associated with Walker-Warburg syndrome, a rare genetic disorder characterized by brain malformations, muscle weakness, and eye abnormalities. Our NGS (Next-Generation Sequencing) genetic testing utilizes advanced sequencing technology to analyze multiple genes simultaneously.
NGS genetic testing for Walker-Warburg syndrome can identify mutations or variants in the CRPPA gene that may be causing the disorder. This information is crucial for diagnosis, prognosis, and genetic counseling. It helps healthcare providers develop personalized treatment plans and provide appropriate support to affected individuals and their families.
Test Name | CRPPA Gene Walker-Warburg syndrome 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 CRPPA Gene Walker-Warburg syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CRPPA Gene Walker-Warburg syndrome |
Test Details |
The CRPPA gene is associated with Walker-Warburg syndrome, which is a rare genetic disorder characterized by a range of symptoms including brain malformations, muscle weakness, and eye abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of Walker-Warburg syndrome, NGS genetic testing can be used to identify mutations or variants in the CRPPA gene that may be causing the disorder. By analyzing the CRPPA gene, NGS genetic testing can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals suspected of having Walker-Warburg syndrome. This information can help healthcare providers develop personalized treatment plans and provide appropriate support to affected individuals and their families. |