SPINOCEREBELLAR ATAXIA COMPREHENSIVE PANEL, EDTA BLOOD

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NABL Cap Accredited   
The Spinocerebellar Ataxia (SCA) Comprehensive Panel analyzes multiple genes known to cause different types of hereditary ataxias. This test helps identify the underlying genetic mutation responsible for progressive coordination and balance problems. Using advanced sequencing and repeat‐expansion analysis, it offers broad and accurate detection. EDTA blood is used to extract DNA, enabling precise diagnosis and guiding management decisions for affected individuals and families

  • 17 Crores+ Samples Processed
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Price: Rs. 16,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: S0001

Frequently Asked Questions (FAQ's):

What does this panel test for?
It screens multiple genes associated with various Spinocerebellar Ataxia subtypes.

Who should undergo this test?
Individuals showing symptoms of ataxia or those with a family history of hereditary ataxias.

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

Does this test detect repeat expansions?
Yes, it includes testing for both sequence variants and repeat expansions linked to SCA.

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

What are the benefits of this panel?
It provides a comprehensive genetic evaluation, enabling accurate diagnosis and aiding in treatment planning.

Can this test help with family planning?
Yes, identifying the causative mutation helps assess genetic risks for family members.

Does Metropolis Healthcare offer this test?
Yes, Metropolis Healthcare provides the SCA Comprehensive Panel using advanced sequencing technologies

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