ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test
At DNA Labs UAE, we offer the ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test. This test helps in diagnosing a rare genetic disorder that affects the development and function of the cerebellum and retina.
Test Details
The ACO2 gene is associated with cerebellar-retinal degeneration, infantile. This disorder is characterized by progressive ataxia (lack of muscle coordination), vision loss, and intellectual disability.
Our NGS (next-generation sequencing) genetic testing method allows us to analyze DNA and detect mutations in the ACO2 gene that may be responsible for cerebellar-retinal degeneration, infantile. This type of testing is crucial for diagnosing the disorder and providing information for genetic counseling and management of the condition.
Components
- Test Name: ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test
- Price: 4400.0 AED
- Sample Condition: Blood
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test type: Ophthalmology Disorders
- Doctor: Ophthalmologist
- Test Department: Genetics
Pre Test Information
Before undergoing the ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test, it is essential 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 by the ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test gene ACO2.
Cost
The ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test is priced at 4400.0 AED.
Test Name | ACO2 Gene Cerebellar-retinal degeneration infantile Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Ophthalmology Disorders |
Doctor | Ophthalmologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for ACO2 Gene Cerebellar-retinal degeneration, infantile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACO2 Gene Cerebellar-retinal degeneration, infantile NGS Genetic DNA Test gene ACO2 |
Test Details |
The ACO2 gene is associated with cerebellar-retinal degeneration, infantile, a rare genetic disorder that affects the development and function of the cerebellum and retina. This disorder is characterized by progressive ataxia (lack of muscle coordination), vision loss, and intellectual disability. NGS (next-generation sequencing) genetic testing is a method of analyzing DNA that can detect mutations in the ACO2 gene that may be responsible for cerebellar-retinal degeneration, infantile. This type of testing can help diagnose the disorder and provide information for genetic counseling and management of the condition. |