Spinocerebellar Ataxia Type 17 Test, Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : No specific preparations, dietary restrictions, or fasting is necessary before providing a blood sample for this test.

₹ 3200

Spinocerebellar Ataxia Type 17 (SCA17) is a rare genetic neurodegenerative disorder characterized by progressively worsening coordination and balance (ataxia). SCA17 is caused by a specific gene mutation and is part of a larger group of genetic ataxia disorders. Genetic testing can confirm the diagnosis and provide valuable information for disease management and family planning.

This guide will answer some of the most commonly asked questions about SCA17 and its implications for you and your family.

Test Name Spinocerebellar Ataxia Type 17 (SCA17)
Sample Type Blood
Preparations Required No specific preparations, dietary restrictions, or fasting is necessary before providing a blood sample for this test.
Report Time 9 Days
Price in Hyderabad ₹ 3200

Why is it important to get a test for SCA17?

Getting a test for SCA17 is crucial if you have a family history of ataxia or are experiencing symptoms like impaired coordination, balance problems, and cognitive decline. Early diagnosis can lead to better management of symptoms and provide information about the risk to other family members.

Is fasting required for the SCA17 test?

No, fasting is not required for the SCA17 genetic test.

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Do I need any specific preparation for the test?

No specific preparation is needed for the SCA17 genetic test.

When should I get this test?

If you exhibit symptoms of ataxia, such as impaired coordination, balance issues, cognitive decline, psychiatric symptoms, and if there's a family history of such symptoms, you should consider getting this test.

What information does the SCA17 genetic test provide?

The SCA17 genetic test identifies the specific mutation associated with SCA17. It can aid in confirming the diagnosis, managing the condition, and understanding the risk to other family members.

How often should I get tested?

The SCA17 genetic test is typically a one-time procedure. However, regular check-ups are necessary to monitor disease progression and manage symptoms.

What are the normal values for this test?

In a genetic test, a normal result indicates the absence of the specific gene mutation associated with SCA17.

What precautions should I take before the test?

There are no specific precautions required for this test. Given the genetic implications of the results, genetic counseling might be beneficial before and after testing.

What factors can affect the results of the test?

The SCA17 genetic test is not influenced by external factors. However, potential laboratory errors or issues with the blood sample could potentially affect the results.

Which doctor should I consult if my test results are abnormal?

If your SCA17 test results are positive, you should consult a neurologist or a genetic counselor.

What happens if my test results are positive?

A positive test result confirms the diagnosis of SCA17. A management plan, which might include physical therapy, medication for psychiatric symptoms or other interventions, can be devised. Genetic counseling can also provide support and information.

Can the SCA17 test be done at home?

No, the SCA17 genetic test requires a blood sample, which should be collected by a healthcare professional and processed in a specialized lab.

Are there any side effects of the SCA17 genetic test?

The SCA17 test involves a standard blood draw, so risks are minimal. However, some people might experience slight pain, bruising, or infection at the injection site.

What does it mean if my test results are negative?

A negative test result means you do not have the specific gene mutation associated with SCA17. However, it does not rule out other types of ataxia or similar disorders.

How reliable is the SCA17 genetic test?

The SCA17 genetic test is highly reliable and accurate when conducted in a credible lab. However, it's always important to discuss your results with a healthcare professional or genetic counselor.

Moving forward, let's understand more about SCA17 and its impact on your life and health.

Can SCA17 be prevented?

Since SCA17 is a genetic disorder, it cannot be prevented if the mutation is present. However, symptoms can be managed, and genetic counseling can provide valuable insights for family planning.

How is SCA17 inherited?

SCA17 is inherited in an autosomal dominant manner, which means an affected person has a 50% chance of passing the mutation to each child.

What are the common symptoms of SCA17?

The symptoms of SCA17 typically include ataxia (poor coordination and balance), cognitive decline, psychiatric symptoms such as depression and irritability, and in some cases, movement disorders like chorea and dystonia.

Can physical therapy help in managing SCA17 symptoms?

Yes, physical therapy can be helpful in managing ataxia and improving coordination and balance. Speech and occupational therapy might also be beneficial.

Are there any specific medications for SCA17?

While there's no cure or specific drug for SCA17, medications can help manage symptoms like movement disorders and psychiatric symptoms. Regular medical check-ups are vital to adjust the treatment plan as needed.

How does SCA17 affect daily life?

SCA17 can make daily tasks challenging due to balance and coordination issues, and cognitive decline. However, with physical therapy and necessary adaptations, individuals with SCA17 can manage daily activities.

How common is SCA17?

SCA17 is a rare form of spinocerebellar ataxia. Its prevalence varies globally, with certain regions having more cases due to specific genetic backgrounds.

Can SCA17 be diagnosed in childhood?

SCA17 typically presents in adulthood, but in rare cases, symptoms can appear in childhood. A genetic test can confirm the diagnosis.

What kind of support is available for individuals with SCA17 and their families?

Support groups, both online and in-person, can provide emotional support and practical advice. Genetic counseling can also be beneficial for affected individuals and their families.

What does current research suggest about the future of SCA17 treatment?

Current research is exploring various approaches to treat SCA17 more effectively, with some looking at ways to stop or reverse the effects of the genetic mutation.

SCA17 is a lifelong journey that requires careful management, but with the right support and treatment, individuals can lead fulfilling lives. Staying informed and connected with healthcare providers is key to managing SCA17 effectively. Remember that while SCA17 is a part of your life, it doesn't define it. Keep embracing your life with strength, resilience, and optimism.

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