Spino Cerebral Ataxia SCA – Single Form Test
Test Name: Spino Cerebral ataxia SCA – Single form Test
Components: EDTA Vacutainer (2ml)
Price: 750.0 AED
Sample Condition: Peripheral blood
Report Delivery: 5-7 days
Method: End Point PCR
Test Type: Genetics
Doctor: General Physician
Test Department:
Pre Test Information: Spino Cerebral ataxia (SCA – Single form) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details
Spino Cerebellar Ataxia (SCA) is a group of genetic disorders characterized by progressive degeneration of the cerebellum and spinal cord. There are several different forms of SCA, each caused by a mutation in a specific gene. However, you specifically mentioned the single form of SCA. It is unclear what you mean by “single form,” as there are multiple subtypes of SCA caused by different gene mutations. Some common subtypes include SCA1, SCA2, SCA3, and SCA6.
Each subtype of SCA has its own unique clinical features, age of onset, and disease progression. However, they all share common symptoms such as progressive ataxia (lack of muscle coordination), balance problems, slurred speech, and difficulty with fine motor skills.
The genetic mutations that cause SCA result in the production of abnormal proteins, which accumulate in certain brain regions and lead to neuronal dysfunction and death. The exact mechanisms of how these mutations cause the specific symptoms and degeneration seen in SCA are still being investigated.
There is currently no cure for SCA, and treatment primarily focuses on managing symptoms and improving quality of life. This may include physical therapy, speech therapy, assistive devices, and medications to control symptoms such as tremors or muscle stiffness.
It is important for individuals with SCA to receive regular medical care and genetic counseling to understand the progression of the disease and its impact on their lives and family members.
| Test Name | Spino Cerebral ataxia SCA – Single form Test |
|---|---|
| Components | EDTA Vacutainer (2ml) |
| Price | 750.0 AED |
| Sample Condition | Peripheral blood |
| Report Delivery | 5-7 days |
| Method | End Point PCR |
| Test type | Genetics |
| Doctor | General Physician |
| Test Department: | |
| Pre Test Information | Spino Cerebral ataxia (SCA – Single form) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details |
Spino Cerebellar Ataxia (SCA) is a group of genetic disorders characterized by progressive degeneration of the cerebellum and spinal cord. There are several different forms of SCA, each caused by a mutation in a specific gene. However, you specifically mentioned the single form of SCA. It is unclear what you mean by “single form,” as there are multiple subtypes of SCA caused by different gene mutations. Some common subtypes include SCA1, SCA2, SCA3, and SCA6. Each subtype of SCA has its own unique clinical features, age of onset, and disease progression. However, they all share common symptoms such as progressive ataxia (lack of muscle coordination), balance problems, slurred speech, and difficulty with fine motor skills. The genetic mutations that cause SCA result in the production of abnormal proteins, which accumulate in certain brain regions and lead to neuronal dysfunction and death. The exact mechanisms of how these mutations cause the specific symptoms and degeneration seen in SCA are still being investigated. There is currently no cure for SCA, and treatment primarily focuses on managing symptoms and improving quality of life. This may include physical therapy, speech therapy, assistive devices, and medications to control symptoms such as tremors or muscle stiffness. It is important for individuals with SCA to receive regular medical care and genetic counseling to understand the progression of the disease and its impact on their lives and family members. |
