SPINOCEREBELLAR ATAXIA 1 (SCA1) DNA DETECTION, EDTA BLOOD

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NABL Cap Accredited     
The SCA1 DNA Detection test identifies abnormal CAG repeat expansions in the ATXN1 gene, which are responsible for Spinocerebellar Ataxia Type 1. This hereditary condition leads to progressive problems with coordination, balance, speech, and motor control. The test uses EDTA blood to extract DNA and accurately determine the repeat size. Early detection helps confirm the diagnosis, guide clinical management, and support genetic counseling for affected families

  • 17 Crores+ Samples Processed
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  • Free Home Collection

Price: Rs. 3,275.00

Sample Type: EDTA BLOOD

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What does the SCA1 DNA test detect?
It identifies CAG repeat expansions in the ATXN1 gene linked to Spinocerebellar Ataxia Type 1.

Who should take this test?
Individuals with symptoms of ataxia or those with a family history of SCA1.

What sample is required?
EDTA blood is needed for DNA extraction.

Does this test confirm the diagnosis?
Yes, it provides a definitive genetic diagnosis for SCA1.

Is fasting required?
No fasting or special preparation is necessary.

How is the result useful?
It helps in early diagnosis, prognosis assessment, and planning appropriate care.

Can family members benefit from testing?
Yes, once a mutation is identified, targeted testing can be offered to relatives.

Does Metropolis Healthcare offer this test?
Yes, Metropolis Healthcare provides SCA1 genetic testing using validated molecular techniques

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