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SCA 1 (Spinocerebellar Ataxia Type -1) Test

Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. This disorder is associated with mutations in the ATXN1 gene, which plays a critical role in nerve cell functions in the brain. The SCA1 test is a genetic test designed to identify these mutations, thus helping to diagnose the condition.


  • Test NameSCA 1 (Spinocerebellar Ataxia Type -1) Test
  • Sample TypeBlood
  • Preparations RequiredThere are no specific instructions for you before taking this test. You do not need to fast or alter your dietary habits.
  • Report Time9 Days

This test can be beneficial to individuals experiencing symptoms related to SCA1, or to those who have a family history of SCA1. The condition is hereditary and is passed down in families in an autosomal dominant manner, meaning that an affected person has a 50% chance of passing the disorder to each of their children.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

The SCA1 test is essential for diagnosing Spinocerebellar Ataxia Type 1. An early diagnosis can help manage the symptoms and plan the necessary care for patients.

No, you do not need to fast for this test. You can eat and drink normally before the test.

If you are experiencing symptoms such as problems with balance, coordination, and speech, or if you have a family history of SCA1, it may be advised to get this test.

This test measures the presence or absence of the mutated ATXN1 gene, which is responsible for causing Spinocerebellar Ataxia Type 1.

As this is a genetic test, it's generally only necessary to have it done once. However, if you have a family history of SCA1, you may choose to have this test repeated, particularly if you plan to have children.

There are no specific precautions necessary for this test. However, because of the significant implications of the results, it is often recommended to consider genetic counseling both before and after the test.

If your test results indicate that you have SCA1, you should consult a neurologist or a genetic counselor. They can guide you through the next steps, which may include further testing, symptom management, and family planning advice.

As this is a genetic test, the results are generally not affected by lifestyle factors. However, certain laboratory errors can lead to a false positive or false negative result.

Genetic testing, such as the SCA1 test, provides valuable insights into an individual's health status and potential genetic disorders. However, it's crucial to understand that positive results can have profound implications. Therefore, it's always recommended to discuss the potential outcomes and implications with a genetic counselor or healthcare provider before undergoing the test. Understanding your genetic health can help you and your healthcare provider make more informed decisions about your medical care and overall well-being.

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